Variant report

Variant	esv33681
Chromosome Location	chr16:30711208-30714408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:0)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr16:30708781-30711645	IMR90	lung:	n/a	chr16:30709461-30709470 chr16:30709865-30709875 chr16:30709332-30709339
2	GABPA	chr16:30709071-30711343	MCF-7	breast:	n/a	chr16:30710025-30710036 chr16:30710022-30710036 chr16:30710025-30710034 chr16:30710433-30710442
3	GABPA	chr16:30710193-30711211	A549	lung:	n/a	chr16:30710433-30710442
4	HCFC1	chr16:30708556-30711606	Hela-S3	cervix:	n/a	n/a
5	JUN	chr16:30712463-30712618	K562	blood:	n/a	n/a
6	JUND	chr16:30712057-30712168	K562	blood:	n/a	n/a
7	KAP1	chr16:30711461-30711649	U2OS	brain:	n/a	n/a
8	MAX	chr16:30711127-30711412	K562	blood:	n/a	n/a
9	MAX	chr16:30709018-30711372	A549	lung:	n/a	chr16:30709729-30709739 chr16:30710135-30710145 chr16:30710431-30710441 chr16:30709439-30709449
10	MAX	chr16:30711068-30711669	K562	blood:	n/a	n/a
11	MAX	chr16:30711863-30712165	K562	blood:	n/a	n/a
12	MAZ	chr16:30708484-30711599	IMR90	lung:	n/a	chr16:30709729-30709739 chr16:30710135-30710145 chr16:30710431-30710441 chr16:30709439-30709449
13	MXI1	chr16:30708677-30712360	SK-N-SH	brain:	n/a	n/a
14	MXI1	chr16:30711179-30711696	K562	blood:	n/a	n/a
15	MYC	chr16:30711213-30711379	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr16:30714381-30714385	K562	blood:	n/a	n/a
17	POLR2A	chr16:30711826-30712267	K562	blood:	n/a	n/a
18	POLR2A	chr16:30709216-30711547	GM12878	blood:	n/a	n/a
19	POLR2A	chr16:30711487-30711499	MCF-7	breast:	n/a	n/a
20	POLR2A	chr16:30709137-30711613	PANC-1	pancreas:	n/a	n/a
21	POLR2A	chr16:30714182-30714379	GM12878	blood:	n/a	n/a
22	POLR2A	chr16:30712442-30712482	HepG2	liver:	n/a	n/a
23	POLR2A	chr16:30711224-30711589	K562	blood:	n/a	n/a
24	POLR2A	chr16:30712570-30712655	K562	blood:	n/a	n/a
25	POLR2A	chr16:30709044-30711209	K562	blood:	n/a	n/a
26	POLR2A	chr16:30713417-30713505	HepG2	liver:	n/a	n/a
27	POLR2A	chr16:30714242-30714278	HepG2	liver:	n/a	n/a
28	POLR2A	chr16:30714192-30714370	K562	blood:	n/a	n/a
29	POLR2A	chr16:30711218-30711223	K562	blood:	n/a	n/a
30	POLR2A	chr16:30711868-30712404	K562	blood:	n/a	n/a
31	POLR2A	chr16:30712541-30712562	K562	blood:	n/a	n/a
32	POLR2A	chr16:30711243-30711421	HepG2	liver:	n/a	n/a
33	POLR2A	chr16:30712761-30713019	GM12878	blood:	n/a	n/a
34	POLR2A	chr16:30713999-30714234	HepG2	liver:	n/a	n/a
35	POLR2A	chr16:30712490-30712506	K562	blood:	n/a	n/a
36	POLR2A	chr16:30714259-30714280	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr16:30712761-30712771	K562	blood:	n/a	n/a
38	POLR2A	chr16:30714213-30714243	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr16:30714279-30714295	HepG2	liver:	n/a	n/a
40	POLR2A	chr16:30713135-30713150	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr16:30712677-30712736	K562	blood:	n/a	n/a
42	SIN3AK20	chr16:30708905-30711215	MCF-7	breast:	n/a	n/a
43	TEAD4	chr16:30709997-30711246	HepG2	liver:	n/a	n/a
44	WRNIP1	chr16:30710462-30711574	GM12878	blood:	n/a	n/a
45	YY1	chr16:30711200-30711411	K562	blood:	n/a	chr16:30711312-30711331
46	ZBTB7A	chr16:30711904-30712233	K562	blood:	n/a	n/a
47	ZNF143	chr16:30711918-30712202	K562	blood:	n/a	chr16:30712033-30712051 chr16:30712040-30712055 chr16:30712037-30712056

No data

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:30660775..30663969-chr16:30709456..30712373,8	K562	blood:
2	chr16:30708909..30711747-chr16:30932178..30935236,6	MCF-7	breast:
3	chr16:30102105..30104221-chr16:30710076..30711578,2	MCF-7	breast:
4	chr16:30708502..30711286-chr16:30712051..30717294,7	K562	blood:
5	chr16:30579675..30583184-chr16:30709142..30711294,3	K562	blood:
6	chr16:30709744..30712013-chr16:30968880..30970502,2	MCF-7	breast:
7	chr16:30707849..30711301-chr16:30785397..30790684,8	K562	blood:
8	chr16:30708929..30712034-chr16:30758251..30761730,4	K562	blood:
9	chr16:30678341..30683972-chr16:30708353..30711640,7	K562	blood:
10	chr16:30667507..30674392-chr16:30704170..30712522,40	MCF-7	breast:
11	chr16:30707963..30711732-chr16:30932569..30936139,6	K562	blood:
12	chr16:30706444..30711338-chr16:30796616..30799537,5	MCF-7	breast:
13	chr16:30708138..30712367-chr16:30742355..30746018,6	K562	blood:
14	chr16:30708356..30712729-chr16:30907440..30911095,7	K562	blood:
15	chr16:30667783..30674540-chr16:30707310..30714065,38	K562	blood:
16	chr16:30660345..30663986-chr16:30707025..30711349,10	K562	blood:
17	chr16:30709500..30711717-chr16:31190248..31191999,2	MCF-7	breast:
18	chr16:30714231..30716333-chr16:30932436..30935145,3	MCF-7	breast:
19	chr16:30708001..30712248-chr16:30758568..30761366,5	K562	blood:
20	chr16:30085772..30087624-chr16:30709718..30711335,2	K562	blood:
21	chr16:30707422..30715768-chr16:30721242..30729414,24	MCF-7	breast:
22	chr16:30660833..30664856-chr16:30708365..30711306,8	MCF-7	breast:
23	chr16:30708760..30712474-chr16:30717976..30728042,17	K562	blood:
24	chr16:30665347..30684079-chr16:30697204..30714344,66	MCF-7	breast:
25	chr16:30707234..30713291-chr16:30747398..30755461,17	MCF-7	breast:
26	chr16:30123424..30125904-chr16:30709036..30711969,2	K562	blood:
27	chr16:30537007..30539690-chr16:30709715..30713303,3	K562	blood:
28	chr16:30708679..30711292-chr16:30884287..30888063,3	MCF-7	breast:
29	chr16:30708050..30711529-chr16:30932244..30936391,8	K562	blood:
30	chr16:30537208..30540827-chr16:30710007..30712078,3	MCF-7	breast:
31	chr16:30707557..30712450-chr16:30785751..30791890,10	K562	blood:
32	chr16:30708936..30712121-chr16:30967511..30970972,5	K562	blood:
33	chr16:30708502..30711286-chr16:30712051..30717294,7	K562	blood:
34	chr16:30707689..30714423-chr16:30749050..30754714,18	MCF-7	breast:
35	chr16:30708426..30712348-chr16:30772033..30775384,7	MCF-7	breast:
36	chr16:30674519..30676444-chr16:30709698..30711527,2	K562	blood:
37	chr16:30369886..30371566-chr16:30709184..30711888,2	MCF-7	breast:
38	chr16:30428007..30431562-chr16:30708422..30711318,5	MCF-7	breast:
39	chr16:30709832..30711688-chr16:30788806..30790347,2	MCF-7	breast:
40	chr16:30709491..30711617-chr16:30777557..30779616,3	K562	blood:
41	chr16:30455606..30458021-chr16:30708271..30711860,5	K562	blood:
42	chr16:30709802..30712559-chr16:30757474..30761628,7	MCF-7	breast:
43	chr16:30388749..30390462-chr16:30709346..30711383,3	MCF-7	breast:
44	chr16:30665738..30673826-chr16:30707321..30713630,33	K562	blood:
45	chr16:30707181..30712037-chr16:30757231..30762842,12	MCF-7	breast:
46	chr16:30710639..30712268-chr16:30903660..30905594,2	MCF-7	breast:
47	chr16:30381749..30384813-chr16:30709284..30711839,3	MCF-7	breast:
48	chr16:30708299..30711208-chr16:30931702..30936734,5	MCF-7	breast:
49	chr16:30536903..30539690-chr16:30709455..30711215,2	K562	blood:
50	chr16:30074678..30077586-chr16:30709449..30711347,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000261840	TF binding region
RNU6-1043P	TF binding region
SRCAP	TF binding region
ENSG00000102886	chromatin interactions
ENSG00000211591	chromatin interactions
ENSG00000260083	chromatin interactions
ENSG00000149922	chromatin interactions
ENSG00000169957	chromatin interactions
ENSG00000156858	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000099381	chromatin interactions
ENSG00000156873	chromatin interactions
ENSG00000199787	chromatin interactions
ENSG00000156860	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000149923	chromatin interactions
ENSG00000222287	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000262026	chromatin interactions
ENSG00000103549	chromatin interactions
ENSG00000099364	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000169221	chromatin interactions
ENSG00000099385	chromatin interactions
ENSG00000196118	chromatin interactions
ENSG00000179965	chromatin interactions
ENSG00000229809	chromatin interactions
ENSG00000206755	chromatin interactions
ENSG00000150281	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000262721	chromatin interactions
ENSG00000265991	chromatin interactions
ENSG00000260852	chromatin interactions
ENSG00000102870	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000260899	chromatin interactions

Extended variants
information (count: 143 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538599578	chr16:30711222-30711223	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	35 gene(s)	Overlapped CNVs	n/a
2	rs557240510	chr16:30711242-30711243	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	35 gene(s)	Overlapped CNVs	n/a
3	rs569415297	chr16:30711309-30711310	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
4	rs144829486	chr16:30711375-30711376	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
5	rs554890151	chr16:30711378-30711379	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
6	rs573368836	chr16:30711400-30711401	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
7	rs148572589	chr16:30711420-30711421	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
8	rs185045609	chr16:30711455-30711456	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
9	rs371665074	chr16:30711487-30711488	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
10	rs577717539	chr16:30711530-30711531	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
11	rs1530203	chr16:30711566-30711567	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563593520	chr16:30711568-30711569	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
13	rs190387479	chr16:30711571-30711572	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
14	rs562360268	chr16:30711577-30711578	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
15	rs535430587	chr16:30711590-30711591	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
16	rs142919651	chr16:30711613-30711614	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
17	rs528281802	chr16:30711630-30711631	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
18	rs150656815	chr16:30711647-30711648	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
19	rs571365407	chr16:30711661-30711662	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
20	rs2972803	chr16:30711682-30711683	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
21	rs550532512	chr16:30711713-30711714	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
22	rs569208204	chr16:30711720-30711721	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
23	rs536576423	chr16:30711725-30711726	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
24	rs532301327	chr16:30711730-30711731	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
25	rs193059478	chr16:30711731-30711732	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
26	rs185878233	chr16:30711754-30711755	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
27	rs145102978	chr16:30711772-30711773	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
28	rs7187691	chr16:30711788-30711789	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs189139092	chr16:30711790-30711791	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
30	rs575163015	chr16:30711817-30711818	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
31	rs73536495	chr16:30711824-30711825	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540950462	chr16:30711843-30711844	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
33	rs180706822	chr16:30711851-30711852	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
34	rs559175194	chr16:30711879-30711880	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
35	rs528283012	chr16:30711880-30711881	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
36	rs540004691	chr16:30711973-30711974	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
37	rs565060960	chr16:30711977-30711978	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
38	rs532495486	chr16:30711990-30711991	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
39	rs185086484	chr16:30711994-30711995	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
40	rs374941133	chr16:30712004-30712005	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
41	rs569194867	chr16:30712012-30712013	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs369654583	chr16:30712018-30712019	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs188432614	chr16:30712019-30712020	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs34438928	chr16:30712028-30712029	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
45	rs370745484	chr16:30712093-30712094	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
46	rs200417893	chr16:30712108-30712109	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
47	rs368667241	chr16:30712131-30712132	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs375018234	chr16:30712137-30712138	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs367593794	chr16:30712178-30712179	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs371783481	chr16:30712188-30712189	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30708800-30711600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr16:30709000-30711400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr16:30709000-30711400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr16:30709000-30711400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr16:30709200-30711400	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr16:30709200-30711400	Active TSS	Esophagus	oesophagus
7	chr16:30709200-30711800	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr16:30709400-30711400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr16:30709400-30711400	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr16:30709400-30711400	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr16:30709400-30711600	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr16:30709600-30711400	Transcr. at gene 5' and 3'	Duodenum Smooth Muscle	Duodenum
13	chr16:30710200-30711400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr16:30710400-30711400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr16:30710400-30711400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr16:30710400-30711400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr16:30710600-30711400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr16:30710600-30711400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
19	chr16:30710600-30711400	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr16:30710600-30711400	Flanking Active TSS	Brain Germinal Matrix	brain
21	chr16:30710600-30711400	Flanking Active TSS	HUVEC	blood vessel
22	chr16:30710600-30711600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr16:30710600-30711600	Flanking Active TSS	Liver	Liver
24	chr16:30710600-30711600	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
25	chr16:30710600-30711600	Transcr. at gene 5' and 3'	Dnd41	blood
26	chr16:30710600-30711800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
27	chr16:30710800-30711400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr16:30710800-30711400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr16:30710800-30711400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr16:30710800-30711400	Flanking Active TSS	Osteobl	bone
31	chr16:30710800-30711600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr16:30710800-30711600	Flanking Active TSS	Rectal Smooth Muscle	rectum
33	chr16:30710800-30711800	Flanking Active TSS	Fetal Heart	heart
34	chr16:30711000-30711400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr16:30711000-30711400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr16:30711000-30711400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr16:30711000-30711400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr16:30711000-30711400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr16:30711000-30711400	Flanking Active TSS	Fetal Kidney	kidney
40	chr16:30711000-30711400	Enhancers	Left Ventricle	heart
41	chr16:30711000-30711400	Enhancers	Lung	lung
42	chr16:30711000-30711400	Weak transcription	Ovary	ovary
43	chr16:30711000-30711400	Flanking Active TSS	GM12878-XiMat	blood
44	chr16:30711000-30711400	Flanking Active TSS	HSMM	muscle
45	chr16:30711000-30711400	Flanking Active TSS	NHDF-Ad	bronchial
46	chr16:30711000-30711600	Genic enhancers	Primary B cells from cord blood	blood
47	chr16:30711000-30711600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr16:30711000-30711600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr16:30711000-30711600	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr16:30711000-30711600	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine

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