Variant report

Variant	nsv933756
Chromosome Location	chr3:81413060-81754738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1932)
CpG islands
(count:183)
Chromatin interactive
region (count:74)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1932 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:81734085-81734232	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:81715746-81715989	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:81725962-81726169	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:81598568-81598974	K562	blood:	n/a	n/a
5	ARID3A	chr3:81525030-81525184	K562	blood:	n/a	n/a
6	ARID3A	chr3:81733986-81734197	K562	blood:	n/a	n/a
7	ARID3A	chr3:81539705-81539945	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:81715726-81716133	K562	blood:	n/a	n/a
9	ARID3A	chr3:81510425-81510561	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:81512022-81512362	HepG2	liver:	n/a	n/a
11	ATF1	chr3:81598619-81598832	K562	blood:	n/a	n/a
12	ATF1	chr3:81733898-81734200	K562	blood:	n/a	n/a
13	ATF1	chr3:81539694-81539966	K562	blood:	n/a	n/a
14	ATF2	chr3:81534488-81535060	GM12878	blood:	n/a	n/a
15	ATF2	chr3:81593386-81593921	GM12878	blood:	n/a	n/a
16	ATF2	chr3:81534486-81534931	GM12878	blood:	n/a	n/a
17	BACH1	chr3:81734002-81734181	K562	blood:	n/a	chr3:81734075-81734089
18	BACH1	chr3:81622912-81622914	K562	blood:	n/a	n/a
19	BATF	chr3:81534550-81535092	GM12878	blood:	n/a	n/a
20	BATF	chr3:81606915-81607180	GM12878	blood:	n/a	n/a
21	BATF	chr3:81717526-81717712	GM12878	blood:	n/a	chr3:81717629-81717640
22	BATF	chr3:81534486-81534834	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:81534515-81534856	GM12878	blood:	n/a	chr3:81534661-81534670
24	BCL3	chr3:81446181-81446476	GM12878	blood:	n/a	n/a
25	BCL3	chr3:81492969-81493465	A549	lung:	n/a	n/a
26	BCLAF1	chr3:81534447-81534951	GM12878	blood:	n/a	chr3:81534661-81534670 chr3:81534899-81534908
27	BHLHE40	chr3:81598621-81598872	K562	blood:	n/a	n/a
28	BHLHE40	chr3:81534564-81534857	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:81733962-81734242	K562	blood:	n/a	n/a
30	BRCA1	chr3:81693047-81693068	H1-hESC	embryonic stem cell:	n/a	n/a
31	CCNT2	chr3:81689401-81689601	K562	blood:	n/a	n/a
32	CCNT2	chr3:81598585-81598820	K562	blood:	n/a	n/a
33	CEBPB	chr3:81692035-81692347	HepG2	liver:	n/a	chr3:81692211-81692222
34	CEBPB	chr3:81427777-81427940	Hela-S3	cervix:	n/a	chr3:81427882-81427893 chr3:81427883-81427892 chr3:81427881-81427894 chr3:81427883-81427892 chr3:81427883-81427892
35	CEBPB	chr3:81751635-81751889	K562	blood:	n/a	chr3:81751814-81751827 chr3:81751814-81751825 chr3:81751815-81751826 chr3:81751814-81751825 chr3:81751814-81751827 chr3:81751813-81751830
36	CEBPB	chr3:81726268-81726581	A549	lung:	n/a	n/a
37	CEBPB	chr3:81445514-81445828	HepG2	liver:	n/a	chr3:81445650-81445661 chr3:81445649-81445662
38	CEBPB	chr3:81629067-81629224	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:81435564-81435756	Hela-S3	cervix:	n/a	chr3:81435672-81435685 chr3:81435673-81435684
40	CEBPB	chr3:81435511-81435812	A549	lung:	n/a	chr3:81435672-81435685 chr3:81435673-81435684
41	CEBPB	chr3:81493093-81493402	A549	lung:	n/a	n/a
42	CEBPB	chr3:81552175-81552736	IMR90	lung:	n/a	chr3:81552320-81552331
43	CEBPB	chr3:81748529-81748733	A549	lung:	n/a	n/a
44	CEBPB	chr3:81492927-81493492	A549	lung:	n/a	n/a
45	CEBPB	chr3:81539661-81540375	IMR90	lung:	n/a	n/a
46	CEBPB	chr3:81413084-81413263	A549	lung:	n/a	chr3:81413130-81413143
47	CEBPB	chr3:81748555-81748760	K562	blood:	n/a	n/a
48	CEBPB	chr3:81539622-81540059	MCF-7	breast:	n/a	n/a
49	CEBPB	chr3:81594909-81595089	A549	lung:	n/a	n/a
50	CEBPB	chr3:81552183-81552467	K562	blood:	n/a	chr3:81552320-81552331

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:81533970-81534020	A549	lung:	n/a
2	chr3:81533970-81534020	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:81533970-81534020	ECC-1	luminal epithelium:	n/a
4	chr3:81604026-81604076	IMR90	lung:	fetal
5	chr3:81540527-81540577	HIPEpiC	eye:	n/a
6	chr3:81540527-81540577	SK-N-SH_RA	brain:	n/a
7	chr3:81533970-81534020	HL-60	blood:	n/a
8	chr3:81604026-81604076	SK-N-MC	brain:	n/a
9	chr3:81604026-81604076	SK-N-SH	brain:	n/a
10	chr3:81604026-81604076	ovcar-3	ovarian:	n/a
11	chr3:81540527-81540577	ECC-1	luminal epithelium:	n/a
12	chr3:81533970-81534020	HCPEpiC	choroid plexus:	n/a
13	chr3:81540527-81540577	HCM	heart:	n/a
14	chr3:81604026-81604076	HRCEpiC	kidney:	n/a
15	chr3:81604026-81604076	NH-A	brain:	n/a
16	chr3:81533970-81534020	HNPCEpiC	eye:	n/a
17	chr3:81533970-81534020	Hepatocyte	liver:	n/a
18	chr3:81540527-81540577	NHBE	bronchial:	n/a
19	chr3:81604026-81604076	HRE	kidney:	n/a
20	chr3:81540527-81540577	HEEpiC	esophagus:	n/a
21	chr3:81604026-81604076	CMK	blood:	n/a
22	chr3:81604026-81604076	MCF10A-Er-Src	breast:	n/a
23	chr3:81540527-81540577	HAEpiC	amniotic membrane:	n/a
24	chr3:81604026-81604076	HRPEpiC	eye:	n/a
25	chr3:81604026-81604076	GM12878	blood:	n/a
26	chr3:81533970-81534020	HMEC	breast:	n/a
27	chr3:81540527-81540577	AoSMC	blood vessel:	n/a
28	chr3:81533970-81534020	AG04450	lung:	fetal
29	chr3:81540527-81540577	HCF	heart:	n/a
30	chr3:81604026-81604076	PFSK-1	brain:	n/a
31	chr3:81533970-81534020	NHDF-neo	bronchial:	n/a
32	chr3:81533970-81534020	Caco-2	colon:	n/a
33	chr3:81540527-81540577	HRCEpiC	kidney:	n/a
34	chr3:81533970-81534020	SK-N-SH_RA	brain:	n/a
35	chr3:81533970-81534020	HEEpiC	esophagus:	n/a
36	chr3:81533970-81534020	SKMC	muscle:	n/a
37	chr3:81533970-81534020	NT2-D1	testis:	n/a
38	chr3:81604026-81604076	HMEC	breast:	n/a
39	chr3:81540527-81540577	NB4	blood:	n/a
40	chr3:81533970-81534020	HepG2	liver:	n/a
41	chr3:81604026-81604076	U87	brain:	n/a
42	chr3:81604026-81604076	BE2_C	brain:	n/a
43	chr3:81540527-81540577	NT2-D1	testis:	n/a
44	chr3:81604026-81604076	SAEC	small airway:	n/a
45	chr3:81604026-81604076	AG09309	skin:	n/a
46	chr3:81540527-81540577	AG10803	skin:	n/a
47	chr3:81533970-81534020	BJ	skin:	n/a
48	chr3:81533970-81534020	LNCaP	prostate:	n/a
49	chr3:81533970-81534020	NHBE	bronchial:	n/a
50	chr3:81533970-81534020	GM12891	blood:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:81630870..81631818-chr3:81692664..81693573,4	MCF-7	breast:
2	chr3:81510208..81513532-chr3:81513585..81516903,3	K562	blood:
3	chr3:81630932..81631818-chr3:81692595..81693468,3	MCF-7	breast:
4	chr3:81751412..81753231-chr3:81755307..81758066,3	K562	blood:
5	chr3:81412721..81414289-chr3:81418366..81420878,2	K562	blood:
6	chr3:81497006..81498618-chr3:81501090..81503352,2	K562	blood:
7	chr3:81497118..81498955-chr3:81501852..81504094,2	K562	blood:
8	chr3:81732924..81735042-chr3:81736495..81738777,2	MCF-7	breast:
9	chr3:81693699..81695612-chr3:81703909..81706890,2	MCF-7	breast:
10	chr3:81732924..81735042-chr3:81736495..81738777,2	MCF-7	breast:
11	chr3:81652021..81654582-chr3:81671146..81673581,2	MCF-7	breast:
12	chr1:247285727..247286228-chr3:81753505..81754005,2	NB4	blood:
13	chr3:81607675..81609561-chr3:81976999..81978516,2	K562	blood:
14	chr3:81504098..81505685-chr3:180830013..180832749,2	MCF-7	breast:
15	chr3:81721733..81724677-chr3:81809908..81812069,2	MCF-7	breast:
16	chr3:81442949..81445413-chr3:81454355..81457016,2	K562	blood:
17	chr3:81468010..81468642-chr3:81539494..81540060,2	MCF-7	breast:
18	chr3:81722096..81724371-chr3:81725223..81727466,2	MCF-7	breast:
19	chr3:81422733..81424855-chr3:81437151..81439095,2	MCF-7	breast:
20	chr3:81441048..81443684-chr3:81443916..81446774,2	MCF-7	breast:
21	chr3:81747836..81749687-chr3:81809960..81812581,3	K562	blood:
22	chr3:81402158..81403031-chr3:81466906..81467495,2	MCF-7	breast:
23	chr18:36266259..36267214-chr3:81430138..81430893,2	MCF-7	breast:
24	chr3:81538877..81541023-chr3:81682087..81685020,2	MCF-7	breast:
25	chr3:81745236..81746984-chr3:81748340..81750520,2	K562	blood:
26	chr3:81609423..81612077-chr3:81612597..81614184,2	K562	blood:
27	chr3:81725205..81727443-chr3:81729973..81731776,2	K562	blood:
28	chr3:81706649..81709647-chr3:81713380..81715113,2	MCF-7	breast:
29	chr3:81412721..81414289-chr3:81418366..81420878,2	K562	blood:
30	chr3:81706649..81709647-chr3:81713380..81715113,2	MCF-7	breast:
31	chr3:81702517..81704180-chr3:81809893..81811884,2	K562	blood:
32	chr17:57120862..57121542-chr3:81600136..81600921,2	MCF-7	breast:
33	chr3:81630870..81631818-chr3:81692664..81693573,4	MCF-7	breast:
34	chr3:81538877..81541023-chr3:81682087..81685020,2	MCF-7	breast:
35	chr3:81350858..81351477-chr3:81692810..81693343,2	MCF-7	breast:
36	chr3:81745236..81746984-chr3:81748340..81750520,2	K562	blood:
37	chr3:81497118..81498955-chr3:81501852..81504094,2	K562	blood:
38	chr3:81609423..81612077-chr3:81612597..81614184,2	K562	blood:
39	chr3:81510208..81513532-chr3:81513585..81516903,3	K562	blood:
40	chr3:81725601..81726395-chr3:81858236..81859143,2	MCF-7	breast:
41	chr3:81652021..81654582-chr3:81671146..81673581,2	MCF-7	breast:
42	chr12:104359580..104360355-chr3:81570763..81571263,2	NB4	blood:
43	chr3:81442949..81445413-chr3:81454355..81457016,2	K562	blood:
44	chr3:81441048..81443684-chr3:81443916..81446774,2	MCF-7	breast:
45	chr3:81725205..81727443-chr3:81729973..81731776,2	K562	blood:
46	chr3:81499173..81502135-chr3:81503844..81505456,2	K562	blood:
47	chr3:81538965..81540197-chr3:81692644..81693504,4	MCF-7	breast:
48	chr17:56735051..56736577-chr3:81662286..81664124,2	MCF-7	breast:
49	chr3:81468046..81468668-chr3:81630873..81631740,2	MCF-7	breast:
50	chr3:81468046..81468668-chr3:81630873..81631740,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ROBO1-7	chr3:81719989-81720133	NONHSAT090617
2	lnc-ROBO1-7	chr3:81703730-81704152	NONHSAT090617
3	lnc-GBE1-7	chr3:81416141-81417172	NONHSAT090613
4	lnc-CADM2-8	chr3:81598550-81598657	ENSG00000249130
5	lnc-CADM2-8	chr3:81597097-81598171	ENSG00000249130
6	lnc-CADM2-8	chr3:81597025-81598649	NONHSAT090615

No data

Variant related genes	Relation type
ENSG00000240404	TF binding region
RNU2-28P	TF binding region
ENSG00000244281	TF binding region
SETP6	TF binding region
GBE1	TF binding region
ENSG00000240404	CpG island
RNU2-28P	CpG island
ENSG00000244281	CpG island
SETP6	CpG island
GBE1	CpG island
ENSG00000139372	chromatin interactions
ENSG00000114480	chromatin interactions
KIAA1598	miRNA target sites
SLC25A22	miRNA target sites

Extended variants
information (count: 10634 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:10634 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539842126	chr3:81413060-81413061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529273928	chr3:81413086-81413087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549321501	chr3:81413108-81413109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183596914	chr3:81413148-81413149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117937980	chr3:81413233-81413234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535273213	chr3:81413265-81413266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542176260	chr3:81413315-81413316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556050836	chr3:81413333-81413334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575731201	chr3:81413334-81413335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11345799	chr3:81413369-81413370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs397990316	chr3:81413379-81413380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376961693	chr3:81413407-81413408	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs369422335	chr3:81413520-81413521	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs532865299	chr3:81413521-81413522	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs275364	chr3:81413562-81413563	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs200577118	chr3:81413612-81413613	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs529158263	chr3:81413621-81413622	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs11443073	chr3:81413630-81413631	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs397990317	chr3:81413636-81413637	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs548985932	chr3:81413674-81413675	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs569166280	chr3:81413714-81413715	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs531525988	chr3:81413724-81413725	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs275365	chr3:81413725-81413726	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs145108049	chr3:81413726-81413727	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs139018820	chr3:81413803-81413804	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs188086159	chr3:81413831-81413832	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs566728687	chr3:81413832-81413833	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs77898795	chr3:81413853-81413854	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs373773391	chr3:81413878-81413879	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs192906705	chr3:81413882-81413883	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs34314911	chr3:81413916-81413917	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs9844025	chr3:81413919-81413920	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs575802873	chr3:81413938-81413939	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs575938254	chr3:81413946-81413947	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs538002572	chr3:81413979-81413980	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557937851	chr3:81413991-81413992	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs74361974	chr3:81414041-81414042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374335140	chr3:81414055-81414056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184511001	chr3:81414065-81414066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565170442	chr3:81414140-81414141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560222476	chr3:81414146-81414147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573541703	chr3:81414173-81414174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542650126	chr3:81414189-81414190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562638086	chr3:81414214-81414215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565056742	chr3:81414255-81414256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77195168	chr3:81414256-81414257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565095256	chr3:81414310-81414311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535879437	chr3:81414321-81414322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533439963	chr3:81414322-81414323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567873209	chr3:81416153-81416154	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:2303 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81400400-81413600	Weak transcription	Aorta	Aorta
2	chr3:81412600-81413400	Enhancers	HUVEC	blood vessel
3	chr3:81412600-81413600	Enhancers	Hela-S3	cervix
4	chr3:81413400-81414000	Flanking Active TSS	HUVEC	blood vessel
5	chr3:81413600-81413800	Enhancers	Aorta	Aorta
6	chr3:81413600-81414000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:81414000-81414400	Enhancers	HUVEC	blood vessel
8	chr3:81423400-81425200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr3:81423600-81424600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:81424000-81424400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr3:81424000-81424600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr3:81424000-81424600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:81424200-81425000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr3:81424200-81425400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr3:81424400-81425000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr3:81424400-81425200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr3:81424600-81425000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr3:81425000-81425400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr3:81425200-81426600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr3:81426600-81426800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr3:81426600-81430000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr3:81427400-81428200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:81427600-81429400	Enhancers	Dnd41	blood
24	chr3:81428200-81428600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:81428600-81430000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:81429000-81429200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr3:81429000-81429400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:81429200-81429600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:81429600-81429800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr3:81432400-81432800	Enhancers	Fetal Brain Female	brain
31	chr3:81432400-81433000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr3:81432800-81435000	Weak transcription	Fetal Brain Male	brain
33	chr3:81432800-81435400	Weak transcription	Fetal Brain Female	brain
34	chr3:81433000-81435600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr3:81435000-81435200	Enhancers	Fetal Brain Male	brain
36	chr3:81435000-81435800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:81435200-81435600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr3:81435200-81435600	Weak transcription	Fetal Brain Male	brain
39	chr3:81435400-81435600	Enhancers	Fetal Brain Female	brain
40	chr3:81435400-81436200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr3:81435600-81436400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr3:81435600-81437400	Enhancers	Fetal Brain Male	brain
43	chr3:81435800-81436600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:81436200-81446600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:81436400-81441400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr3:81437400-81442600	Weak transcription	Fetal Brain Male	brain
47	chr3:81439600-81440600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:81440000-81440400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:81441400-81445800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr3:81442000-81445200	Enhancers	Brain Germinal Matrix	brain

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