Variant report

Variant	nsv470014
Chromosome Location	chr4:8390646-8429817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1406)
CpG islands
(count:1591)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8412338-8412758	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:8412399-8412649	K562	blood:	n/a	n/a
3	ARID3A	chr4:8404836-8405202	K562	blood:	n/a	n/a
4	ATF1	chr4:8412326-8412570	K562	blood:	n/a	n/a
5	ATF2	chr4:8393604-8394136	GM12878	blood:	n/a	n/a
6	ATF2	chr4:8421154-8421641	GM12878	blood:	n/a	n/a
7	ATF2	chr4:8421093-8421717	GM12878	blood:	n/a	n/a
8	ATF2	chr4:8393632-8394071	GM12878	blood:	n/a	n/a
9	ATF3	chr4:8394650-8394856	K562	blood:	n/a	n/a
10	BACH1	chr4:8410445-8410646	K562	blood:	n/a	n/a
11	BACH1	chr4:8412181-8412692	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:8421214-8421458	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:8421183-8421487	K562	blood:	n/a	n/a
14	BACH1	chr4:8412326-8412529	K562	blood:	n/a	n/a
15	BATF	chr4:8393629-8394080	GM12878	blood:	n/a	chr4:8393850-8393861
16	BATF	chr4:8395274-8395671	GM12878	blood:	n/a	n/a
17	BATF	chr4:8393671-8394070	GM12878	blood:	n/a	chr4:8393850-8393861
18	BATF	chr4:8421176-8421733	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:8395270-8395502	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:8393722-8394039	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:8393709-8394001	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:8421129-8421607	GM12878	blood:	n/a	n/a
23	BCL3	chr4:8393673-8394086	GM12878	blood:	n/a	n/a
24	BCL3	chr4:8392791-8393336	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:8393699-8394095	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:8393674-8394053	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:8420591-8420811	K562	blood:	n/a	n/a
28	BHLHE40	chr4:8421192-8421946	K562	blood:	n/a	n/a
29	BHLHE40	chr4:8404998-8405197	K562	blood:	n/a	n/a
30	BHLHE40	chr4:8429685-8430385	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:8421201-8421716	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:8395256-8395626	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:8412342-8412781	K562	blood:	n/a	n/a
34	BHLHE40	chr4:8429740-8430403	HepG2	liver:	n/a	n/a
35	BHLHE40	chr4:8429729-8430434	K562	blood:	n/a	n/a
36	BHLHE40	chr4:8402825-8403047	K562	blood:	n/a	n/a
37	BRCA1	chr4:8404917-8405277	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr4:8405512-8405630	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr4:8392996-8393002	GM12878	blood:	n/a	n/a
40	BRCA1	chr4:8429722-8429863	GM12878	blood:	n/a	n/a
41	CBX3	chr4:8428504-8428852	K562	blood:	n/a	n/a
42	CBX3	chr4:8408643-8408942	K562	blood:	n/a	n/a
43	CCNT2	chr4:8404994-8405220	K562	blood:	n/a	n/a
44	CEBPB	chr4:8421020-8421447	K562	blood:	n/a	n/a
45	CEBPB	chr4:8394317-8394537	IMR90	lung:	n/a	chr4:8394384-8394395
46	CEBPB	chr4:8401325-8401528	K562	blood:	n/a	chr4:8401458-8401469
47	CEBPB	chr4:8402175-8402475	IMR90	lung:	n/a	chr4:8402338-8402349
48	CEBPB	chr4:8391613-8392104	IMR90	lung:	n/a	chr4:8391780-8391791
49	CEBPB	chr4:8424095-8424458	MCF-7	breast:	n/a	n/a
50	CEBPB	chr4:8391613-8391995	HepG2	liver:	n/a	chr4:8391780-8391791

(count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8396056-8396106	HCM	heart:	n/a
2	chr4:8418132-8418182	AG09319	gingival:	n/a
3	chr4:8412549-8412599	SK-N-SH_RA	brain:	n/a
4	chr4:8418132-8418182	HRCEpiC	kidney:	n/a
5	chr4:8405046-8405096	HRE	kidney:	n/a
6	chr4:8396056-8396106	HCM	heart:	n/a
7	chr4:8418132-8418182	AG09319	gingival:	n/a
8	chr4:8412549-8412599	SK-N-SH_RA	brain:	n/a
9	chr4:8418132-8418182	HRCEpiC	kidney:	n/a
10	chr4:8405046-8405096	HRE	kidney:	n/a
11	chr4:8399409-8399459	HRPEpiC	eye:	n/a
12	chr4:8399320-8399370	Hela-S3	cervix:	n/a
13	chr4:8412795-8412845	IMR90	lung:	fetal
14	chr4:8390837-8390887	AG04450	lung:	fetal
15	chr4:8405046-8405096	SAEC	small airway:	n/a
16	chr4:8412795-8412845	HRPEpiC	eye:	n/a
17	chr4:8409270-8409320	ProgFib	skin:	n/a
18	chr4:8396056-8396106	T-47D	breast:	n/a
19	chr4:8399320-8399370	ECC-1	luminal epithelium:	n/a
20	chr4:8418050-8418100	HRCEpiC	kidney:	n/a
21	chr4:8395941-8395991	CMK	blood:	n/a
22	chr4:8418050-8418100	A549	lung:	n/a
23	chr4:8418132-8418182	HAEpiC	amniotic membrane:	n/a
24	chr4:8409270-8409320	Caco-2	colon:	n/a
25	chr4:8396056-8396106	GM12892	blood:	n/a
26	chr4:8396502-8396552	HRCEpiC	kidney:	n/a
27	chr4:8398880-8398930	AG09309	skin:	n/a
28	chr4:8399320-8399370	RPTEC	kidney:	n/a
29	chr4:8396502-8396552	GM12891	blood:	n/a
30	chr4:8409328-8409378	Hela-S3	cervix:	n/a
31	chr4:8412369-8412419	AG04449	skin:	fetal
32	chr4:8418006-8418056	T-47D	breast:	n/a
33	chr4:8398880-8398930	K562	blood:	n/a
34	chr4:8399409-8399459	GM12878	blood:	n/a
35	chr4:8398737-8398787	NHDF-neo	bronchial:	n/a
36	chr4:8412795-8412845	CMK	blood:	n/a
37	chr4:8412736-8412786	SK-N-SH_RA	brain:	n/a
38	chr4:8390837-8390887	HRCEpiC	kidney:	n/a
39	chr4:8418050-8418100	AG04450	lung:	fetal
40	chr4:8396056-8396106	SK-N-MC	brain:	n/a
41	chr4:8399320-8399370	SAEC	small airway:	n/a
42	chr4:8418050-8418100	AG10803	skin:	n/a
43	chr4:8399320-8399370	T-47D	breast:	n/a
44	chr4:8390837-8390887	H1-hESC	embryonic stem cell:	embryo
45	chr4:8398823-8398873	PANC-1	pancreas:	n/a
46	chr4:8399409-8399459	HCM	heart:	n/a
47	chr4:8398737-8398787	K562	blood:	n/a
48	chr4:8390837-8390887	HMEC	breast:	n/a
49	chr4:8429229-8429279	HL-60	blood:	n/a
50	chr4:8412736-8412786	CMK	blood:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8243593..8244617-chr4:8404301..8405948,10	MCF-7	breast:
2	chr4:8243635..8244141-chr4:8412098..8412912,2	K562	blood:
3	chr4:8414211..8417979-chr4:8429248..8432423,3	MCF-7	breast:
4	chr4:8411333..8413116-chr4:8429011..8431079,2	MCF-7	breast:
5	chr4:8244036..8244570-chr4:8408366..8408880,3	K562	blood:
6	chr4:8405868..8408180-chr4:8410385..8411900,2	K562	blood:
7	chr4:8416707..8419298-chr4:8428396..8430193,3	MCF-7	breast:
8	chr4:8404879..8407755-chr4:8409696..8411552,2	MCF-7	breast:
9	chr4:8412663..8414756-chr4:8414899..8416895,2	K562	blood:
10	chr4:8247640..8250580-chr4:8396679..8398196,2	K562	blood:
11	chr4:8276309..8277181-chr4:8404667..8405454,2	MCF-7	breast:
12	chr4:8389242..8391252-chr4:8392488..8394168,2	MCF-7	breast:
13	chr4:8412667..8415883-chr4:8441026..8444173,3	K562	blood:
14	chr4:8243586..8244597-chr4:8404569..8406088,15	MCF-7	breast:
15	chr4:8268241..8269567-chr4:8404622..8405485,4	MCF-7	breast:
16	chr4:8404879..8407755-chr4:8409696..8411552,2	MCF-7	breast:
17	chr4:8401144..8403051-chr4:8405027..8406655,2	MCF-7	breast:
18	chr4:8243670..8244249-chr4:8412115..8412989,3	MCF-7	breast:
19	chr4:8268685..8271204-chr4:8420095..8422355,2	MCF-7	breast:
20	chr4:8419092..8423241-chr4:8430004..8433236,3	MCF-7	breast:
21	chr4:8268620..8269557-chr4:8404343..8405485,5	K562	blood:
22	chr4:8276769..8277333-chr4:8404587..8405165,2	K562	blood:
23	chr4:8405868..8408180-chr4:8410385..8411900,2	K562	blood:
24	chr4:8321841..8322735-chr4:8404626..8405371,2	MCF-7	breast:
25	chr4:8252940..8255402-chr4:8411571..8414054,2	K562	blood:
26	chr4:8321843..8322383-chr4:8404924..8405518,2	MCF-7	breast:
27	chr4:8411216..8414170-chr4:8427431..8430219,2	MCF-7	breast:
28	chr4:8416707..8419298-chr4:8428396..8430193,3	MCF-7	breast:
29	chr4:8410214..8413644-chr4:8429714..8431536,3	K562	blood:
30	chr4:8401612..8405935-chr4:8442501..8444816,3	MCF-7	breast:
31	chr4:8414211..8417979-chr4:8429248..8432423,3	MCF-7	breast:
32	chr4:8243862..8244409-chr4:8407695..8408313,2	MCF-7	breast:
33	chr4:8401144..8403051-chr4:8405027..8406655,2	MCF-7	breast:
34	chr4:8395997..8397565-chr4:8399948..8402070,2	K562	blood:
35	chr4:8428067..8433323-chr4:8440948..8445760,8	K562	blood:
36	chr4:8429518..8431924-chr4:8437588..8440150,2	MCF-7	breast:
37	chr4:8428810..8430394-chr4:8440724..8444143,3	K562	blood:
38	chr4:8243135..8244560-chr4:8404576..8405520,11	K562	blood:
39	chr4:8412508..8416486-chr4:8417537..8419661,3	MCF-7	breast:
40	chr4:8268593..8269552-chr4:8403907..8405561,11	MCF-7	breast:
41	chr4:8404571..8406655-chr4:8410577..8413639,3	MCF-7	breast:
42	chr4:8389242..8391252-chr4:8392488..8394168,2	MCF-7	breast:
43	chr4:8243346..8245051-chr4:8408250..8411036,2	K562	blood:
44	chr4:8393388..8395511-chr4:8408173..8409725,2	MCF-7	breast:
45	chr4:8429704..8431761-chr4:8439023..8440743,2	MCF-7	breast:
46	chr4:8404571..8406655-chr4:8410577..8413639,3	MCF-7	breast:
47	chr4:8385368..8387475-chr4:8389606..8391227,2	MCF-7	breast:
48	chr4:8276397..8277253-chr4:8404609..8405203,3	MCF-7	breast:
49	chr4:8421637..8423534-chr4:8447080..8448932,2	K562	blood:
50	chr4:8429725..8430462-chrX:12992795..12993539,2	HCT-116	colon:

No data

Variant related genes	Relation type
ACOX3	TF binding region
RNA5SP152	TF binding region
ACOX3	CpG island
RNA5SP152	CpG island
ENSG00000155275	chromatin interactions
ENSG00000248986	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000205542	chromatin interactions
ENSG00000249145	chromatin interactions
ENSG00000202054	chromatin interactions

Extended variants
information (count: 2027 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2027 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1568692	chr4:8390646-8390647	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374690682	chr4:8390674-8390675	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181301633	chr4:8390678-8390679	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186506604	chr4:8390701-8390702	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527243304	chr4:8390751-8390752	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73799167	chr4:8390752-8390753	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs561005991	chr4:8390759-8390760	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531417132	chr4:8390778-8390779	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550424228	chr4:8390797-8390798	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530752406	chr4:8390798-8390799	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571839254	chr4:8390802-8390803	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139709179	chr4:8390825-8390826	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143888158	chr4:8390858-8390859	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs13136987	chr4:8390859-8390860	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs113317365	chr4:8390880-8390881	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs146891905	chr4:8390903-8390904	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548170046	chr4:8390918-8390919	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370874561	chr4:8390929-8390930	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13434465	chr4:8390948-8390949	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs113402127	chr4:8390958-8390959	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142001570	chr4:8390965-8390966	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs202154683	chr4:8390967-8390968	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145751243	chr4:8390972-8390973	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138564245	chr4:8390979-8390980	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115146093	chr4:8390991-8390992	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201425518	chr4:8390992-8390993	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114126152	chr4:8390998-8390999	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs138860196	chr4:8390999-8391000	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs554082211	chr4:8391039-8391040	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572242062	chr4:8391043-8391044	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2242483	chr4:8391049-8391050	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs202006899	chr4:8391063-8391064	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs16842165	chr4:8391119-8391120	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs543507124	chr4:8391120-8391121	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555256838	chr4:8391137-8391138	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs36055234	chr4:8391165-8391166	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368490039	chr4:8391188-8391189	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532690394	chr4:8391200-8391201	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144357499	chr4:8391201-8391202	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs57692256	chr4:8391251-8391252	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530316561	chr4:8391275-8391276	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs114372559	chr4:8391298-8391299	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs372482219	chr4:8391310-8391311	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201011526	chr4:8391317-8391318	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs552214471	chr4:8391321-8391322	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs149402565	chr4:8391338-8391339	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs201816216	chr4:8391339-8391340	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs113578128	chr4:8391340-8391341	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs116406348	chr4:8391358-8391359	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112332730	chr4:8391382-8391383	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1931 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8360400-8394000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:8360400-8395600	Weak transcription	NHEK	skin
3	chr4:8362000-8395400	Weak transcription	Fetal Brain Male	brain
4	chr4:8364800-8392400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:8366400-8411600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr4:8373400-8401600	Strong transcription	Fetal Intestine Small	intestine
7	chr4:8375000-8401600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr4:8378000-8391800	Strong transcription	Fetal Brain Female	brain
9	chr4:8378600-8398600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:8378600-8398800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr4:8378800-8397800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr4:8379000-8395400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:8379400-8392000	Strong transcription	Brain Hippocampus Middle	brain
14	chr4:8381000-8393800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:8381600-8392400	Strong transcription	Brain Cingulate Gyrus	brain
16	chr4:8381800-8394400	Strong transcription	Brain Germinal Matrix	brain
17	chr4:8381800-8398600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr4:8382400-8401600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:8383800-8419000	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr4:8384000-8394600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:8384000-8395600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:8384000-8399600	Strong transcription	Spleen	Spleen
23	chr4:8384800-8391000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:8384800-8392000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr4:8384800-8401600	Strong transcription	Thymus	Thymus
26	chr4:8384800-8418600	Strong transcription	Primary T cells from cord blood	blood
27	chr4:8385200-8395200	Weak transcription	Fetal Kidney	kidney
28	chr4:8385200-8411600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr4:8385400-8395600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:8385600-8392400	Strong transcription	Stomach Smooth Muscle	stomach
31	chr4:8385600-8407000	Weak transcription	Stomach Mucosa	stomach
32	chr4:8385800-8391200	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr4:8386000-8393400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:8386200-8391400	Strong transcription	Brain Angular Gyrus	brain
35	chr4:8386200-8392200	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr4:8386400-8391400	Strong transcription	Gastric	stomach
37	chr4:8386400-8392400	Weak transcription	GM12878-XiMat	blood
38	chr4:8386400-8393000	Strong transcription	Fetal Stomach	stomach
39	chr4:8386400-8398200	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr4:8386400-8408400	Strong transcription	Fetal Intestine Large	intestine
41	chr4:8386600-8393400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr4:8386600-8398600	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr4:8386600-8399400	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr4:8386600-8400600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr4:8386800-8391800	Strong transcription	Primary B cells from cord blood	blood
46	chr4:8386800-8393000	Strong transcription	Adipose Nuclei	Adipose
47	chr4:8386800-8393000	Strong transcription	Rectal Smooth Muscle	rectum
48	chr4:8386800-8396600	Strong transcription	Lung	lung
49	chr4:8387000-8391600	Strong transcription	Colonic Mucosa	Colon
50	chr4:8387000-8392800	Strong transcription	Brain Anterior Caudate	brain

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