Variant report

Variant	esv12842
Chromosome Location	chr8:8749942-8751417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:8751036-8751247	GM12878	blood:	n/a	chr8:8751163-8751183
2	ATF3	chr8:8750940-8751242	GM12878	blood:	n/a	chr8:8751163-8751183
3	ATF3	chr8:8750978-8751243	H1-hESC	embryonic stem cell:	n/a	chr8:8751163-8751183
4	ATF3	chr8:8750978-8751250	K562	blood:	n/a	chr8:8751163-8751183
5	ATF3	chr8:8750950-8751310	HepG2	liver:	n/a	chr8:8751163-8751183
6	BACH1	chr8:8751377-8751489	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:8751398-8751562	K562	blood:	n/a	n/a
8	BCLAF1	chr8:8750870-8751214	GM12878	blood:	n/a	chr8:8751147-8751160 chr8:8750943-8750956
9	BHLHE40	chr8:8750995-8751344	HepG2	liver:	n/a	chr8:8751138-8751154 chr8:8751144-8751160 chr8:8751161-8751174
10	BHLHE40	chr8:8750339-8750646	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:8750970-8751320	GM12878	blood:	n/a	chr8:8751138-8751154 chr8:8751144-8751160 chr8:8751161-8751174
12	BHLHE40	chr8:8750981-8751590	K562	blood:	n/a	chr8:8751138-8751154 chr8:8751144-8751160 chr8:8751161-8751174
13	BHLHE40	chr8:8750308-8750515	K562	blood:	n/a	n/a
14	BRCA1	chr8:8751348-8751425	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr8:8750298-8751487	K562	blood:	n/a	n/a
16	CEBPD	chr8:8750872-8751206	HepG2	liver:	n/a	n/a
17	CHD1	chr8:8751088-8751115	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr8:8749977-8750570	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr8:8750843-8751239	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr8:8750408-8750567	GM12878	blood:	n/a	n/a
21	CHD2	chr8:8751396-8751565	K562	blood:	n/a	n/a
22	CHD2	chr8:8749654-8750359	Hela-S3	cervix:	n/a	n/a
23	CREB1	chr8:8750429-8750881	A549	lung:	n/a	n/a
24	CREB1	chr8:8750955-8751370	A549	lung:	n/a	n/a
25	CTCF	chr8:8750650-8750788	GM10248	blood:	n/a	n/a
26	CTCF	chr8:8749980-8750130	HMEC	breast:	n/a	n/a
27	CTCF	chr8:8749968-8750023	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:8750689-8750844	GM12892	blood:	n/a	n/a
29	CTCF	chr8:8750636-8750791	GM12891	blood:	n/a	n/a
30	CTCF	chr8:8750400-8750550	GM12864	blood:	n/a	n/a
31	CTCF	chr8:8751060-8751210	GM12871	blood:	n/a	chr8:8751142-8751155
32	CTCF	chr8:8751040-8751190	HMEC	breast:	n/a	chr8:8751142-8751155
33	CTCF	chr8:8751086-8751188	MCF-7	breast:	n/a	chr8:8751142-8751155
34	CTCF	chr8:8751040-8751229	GM12891	blood:	n/a	chr8:8751142-8751155
35	CTCF	chr8:8750200-8750350	HepG2	liver:	n/a	n/a
36	CTCF	chr8:8751130-8751167	MCF-7	breast:	n/a	chr8:8751142-8751155
37	CTCF	chr8:8751089-8751235	Pancreas_OC	pancreas:	n/a	chr8:8751142-8751155
38	CTCF	chr8:8751095-8751205	MCF-7	breast:	n/a	chr8:8751142-8751155
39	CTCF	chr8:8751080-8751370	GM12870	blood:	n/a	chr8:8751332-8751341 chr8:8751328-8751341 chr8:8751142-8751155
40	CTCF	chr8:8751300-8751450	HUVEC	blood vessel:	n/a	chr8:8751332-8751341 chr8:8751328-8751341
41	CTCF	chr8:8750740-8750890	AG04449	skin:	n/a	n/a
42	CTCF	chr8:8751079-8751206	Lung_OC	lung:	n/a	chr8:8751142-8751155
43	CTCF	chr8:8751082-8751233	Spleen_OC	spleen:	n/a	chr8:8751142-8751155
44	CTCF	chr8:8750160-8750310	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr8:8751127-8751193	HUVEC	blood vessel:	n/a	chr8:8751142-8751155
46	CTCF	chr8:8750414-8750484	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr8:8751060-8751210	GM12869	blood:	n/a	chr8:8751142-8751155
48	CTCF	chr8:8750720-8750870	GM12869	blood:	n/a	n/a
49	CTCF	chr8:8749958-8750077	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:8750760-8750910	GM12874	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8750314-8750364	GM12891	blood:	n/a
2	chr8:8751409-8751459	NHBE	bronchial:	n/a
3	chr8:8750314-8750364	T-47D	breast:	n/a
4	chr8:8749938-8749988	AG09319	gingival:	n/a
5	chr8:8751409-8751459	Hepatocyte	liver:	n/a
6	chr8:8750517-8750567	CMK	blood:	n/a
7	chr8:8750517-8750567	HCT-116	colon:	n/a
8	chr8:8749919-8749969	HRCEpiC	kidney:	n/a
9	chr8:8750517-8750567	SAEC	small airway:	n/a
10	chr8:8751325-8751375	AG09309	skin:	n/a
11	chr8:8750517-8750567	HCM	heart:	n/a
12	chr8:8750517-8750567	AG10803	skin:	n/a
13	chr8:8749919-8749969	MCF-7	breast:	n/a
14	chr8:8749938-8749988	MCF-7	breast:	n/a
15	chr8:8750314-8750364	Hela-S3	cervix:	n/a
16	chr8:8750517-8750567	ProgFib	skin:	n/a
17	chr8:8749919-8749969	ProgFib	skin:	n/a
18	chr8:8750314-8750364	NT2-D1	testis:	n/a
19	chr8:8749938-8749988	HRE	kidney:	n/a
20	chr8:8750517-8750567	HAEpiC	amniotic membrane:	n/a
21	chr8:8750314-8750364	Caco-2	colon:	n/a
22	chr8:8750517-8750567	NHDF-neo	bronchial:	n/a
23	chr8:8749938-8749988	BJ	skin:	n/a
24	chr8:8749919-8749969	AG04450	lung:	fetal
25	chr8:8750314-8750364	HIPEpiC	eye:	n/a
26	chr8:8749919-8749969	HUVEC	blood vessel:	n/a
27	chr8:8750314-8750364	HCT-116	colon:	n/a
28	chr8:8750314-8750364	ECC-1	luminal epithelium:	n/a
29	chr8:8750517-8750567	HepG2	liver:	n/a
30	chr8:8751409-8751459	GM12892	blood:	n/a
31	chr8:8750314-8750364	HAEpiC	amniotic membrane:	n/a
32	chr8:8750517-8750567	Hela-S3	cervix:	n/a
33	chr8:8751409-8751459	BE2_C	brain:	n/a
34	chr8:8751325-8751375	SAEC	small airway:	n/a
35	chr8:8750517-8750567	PFSK-1	brain:	n/a
36	chr8:8749919-8749969	T-47D	breast:	n/a
37	chr8:8751325-8751375	SKMC	muscle:	n/a
38	chr8:8750314-8750364	CMK	blood:	n/a
39	chr8:8750517-8750567	HRPEpiC	eye:	n/a
40	chr8:8750517-8750567	K562	blood:	n/a
41	chr8:8751409-8751459	HEK293	kidney:	embryo
42	chr8:8751325-8751375	HIPEpiC	eye:	n/a
43	chr8:8751325-8751375	BJ	skin:	n/a
44	chr8:8751325-8751375	GM06990	blood:	n/a
45	chr8:8751325-8751375	CMK	blood:	n/a
46	chr8:8749919-8749969	GM12891	blood:	n/a
47	chr8:8751409-8751459	NH-A	brain:	n/a
48	chr8:8750517-8750567	HRCEpiC	kidney:	n/a
49	chr8:8749938-8749988	HNPCEpiC	eye:	n/a
50	chr8:8749919-8749969	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:8748349..8752697-chr8:8864961..8869329,4	K562	blood:
2	chr8:8715858..8717945-chr8:8749655..8752629,2	K562	blood:
3	chr8:8647143..8649997-chr8:8748170..8750908,2	MCF-7	breast:
4	chr8:8678976..8682016-chr8:8748981..8752043,3	MCF-7	breast:
5	chr8:8637079..8641758-chr8:8747812..8752273,5	MCF-7	breast:
6	chr8:8676467..8679551-chr8:8749550..8751180,3	K562	blood:
7	chr8:8678713..8680298-chr8:8749363..8750992,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-682P	TF binding region
MFHAS1	TF binding region
RNU6-682P	CpG island
MFHAS1	CpG island
ENSG00000147324	chromatin interactions
ENSG00000254367	chromatin interactions
ENSG00000104626	chromatin interactions

Extended variants
information (count: 71 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147391131	chr8:8749944-8749945	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs61745486	chr8:8749945-8749946	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs75762619	chr8:8749965-8749966	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs377473219	chr8:8749981-8749982	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs370850957	chr8:8749985-8749986	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs35036539	chr8:8749990-8749991	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs144903843	chr8:8750005-8750006	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs200214807	chr8:8750015-8750016	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs148791373	chr8:8750019-8750020	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs369037183	chr8:8750031-8750032	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs201865659	chr8:8750037-8750038	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs553512553	chr8:8750070-8750071	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs34984230	chr8:8750082-8750083	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs61740135	chr8:8750113-8750114	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs151297285	chr8:8750125-8750126	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs545590091	chr8:8750132-8750133	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs199669294	chr8:8750143-8750144	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs140687607	chr8:8750152-8750153	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs375796811	chr8:8750155-8750156	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs541714002	chr8:8750217-8750218	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs376520770	chr8:8750244-8750245	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs141278509	chr8:8750245-8750246	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs527602701	chr8:8750265-8750266	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs371432144	chr8:8750268-8750269	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs376081159	chr8:8750283-8750284	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs546555633	chr8:8750285-8750286	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs371656093	chr8:8750299-8750300	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs145797270	chr8:8750330-8750331	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs115597655	chr8:8750333-8750334	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs374041668	chr8:8750353-8750354	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs201309261	chr8:8750391-8750392	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs569422501	chr8:8750409-8750410	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs538473476	chr8:8750413-8750414	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs547497962	chr8:8750416-8750417	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs200720299	chr8:8750425-8750426	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs555281714	chr8:8750432-8750433	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs367889110	chr8:8750434-8750435	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs566247640	chr8:8750440-8750441	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs534516012	chr8:8750465-8750466	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs1062988	chr8:8750467-8750468	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs576766983	chr8:8750576-8750577	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs372812955	chr8:8750670-8750671	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs539518189	chr8:8750734-8750735	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs556027176	chr8:8750742-8750743	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs575809107	chr8:8750748-8750749	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs541594536	chr8:8750768-8750769	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs561559305	chr8:8750795-8750796	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs571965955	chr8:8750806-8750807	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs540970630	chr8:8750815-8750816	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs3110411	chr8:8750901-8750902	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Gastric cancer	17229543	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8745200-8750200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
2	chr8:8745800-8750600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
3	chr8:8747200-8750200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
4	chr8:8747400-8750000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:8747600-8750200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
6	chr8:8747600-8750200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr8:8747800-8751800	Active TSS	Fetal Kidney	kidney
8	chr8:8748200-8750000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
9	chr8:8748200-8750000	Enhancers	Fetal Heart	heart
10	chr8:8748600-8750400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
11	chr8:8748800-8750000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
12	chr8:8748800-8750000	Flanking Active TSS	Right Ventricle	heart
13	chr8:8748800-8750400	Flanking Active TSS	Stomach Smooth Muscle	stomach
14	chr8:8748800-8750600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
15	chr8:8749000-8750000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr8:8749000-8750000	Enhancers	Primary B cells from peripheral blood	blood
17	chr8:8749000-8750000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr8:8749000-8750000	Flanking Active TSS	Brain Substantia Nigra	brain
19	chr8:8749000-8750000	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr8:8749000-8750200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:8749000-8750200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:8749000-8750200	Flanking Active TSS	Fetal Thymus	thymus
23	chr8:8749000-8750400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr8:8749000-8750600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
25	chr8:8749000-8750600	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr8:8749200-8750000	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:8749200-8750000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:8749200-8750000	Flanking Active TSS	Brain Angular Gyrus	brain
29	chr8:8749200-8750000	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr8:8749200-8750000	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr8:8749200-8750000	Flanking Active TSS	Gastric	stomach
32	chr8:8749200-8750000	Flanking Active TSS	Lung	lung
33	chr8:8749200-8750200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr8:8749200-8750200	Flanking Active TSS	Brain Germinal Matrix	brain
35	chr8:8749200-8750200	Flanking Active TSS	NH-A	brain
36	chr8:8749200-8750400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:8749200-8750400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr8:8749200-8750400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr8:8749200-8750600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:8749200-8750600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:8749200-8750600	Flanking Active TSS	Esophagus	oesophagus
42	chr8:8749200-8750800	Flanking Active TSS	HMEC	breast
43	chr8:8749200-8751800	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr8:8749400-8750000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr8:8749400-8750000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:8749400-8750000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:8749400-8750000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr8:8749400-8750000	Flanking Active TSS	Fetal Brain Female	brain
49	chr8:8749400-8750000	Flanking Active TSS	Fetal Intestine Large	intestine
50	chr8:8749400-8750000	Flanking Active TSS	Fetal Intestine Small	intestine

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