Variant report

Variant	esv1798120
Chromosome Location	chr6:25136860-25149538
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:372)
CpG islands
(count:797)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:25138444-25138722	K562	blood:	n/a	n/a
2	ATF2	chr6:25137739-25139485	GM12878	blood:	n/a	n/a
3	ATF2	chr6:25138138-25139054	GM12878	blood:	n/a	n/a
4	ATF2	chr6:25147259-25147841	GM12878	blood:	n/a	n/a
5	BATF	chr6:25138903-25139261	GM12878	blood:	n/a	n/a
6	BATF	chr6:25138159-25138751	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:25138247-25138752	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:25147298-25147929	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:25138131-25139253	GM12878	blood:	n/a	chr6:25139184-25139193
10	BHLHE40	chr6:25147488-25147755	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:25138008-25138134	GM12878	blood:	n/a	n/a
12	CEBPB	chr6:25137797-25138153	A549	lung:	n/a	n/a
13	CEBPB	chr6:25137779-25139523	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:25137782-25139143	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:25137713-25139611	GM12878	blood:	n/a	n/a
16	CEBPB	chr6:25137793-25138137	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:25137795-25138133	K562	blood:	n/a	n/a
18	CHD1	chr6:25138115-25139561	GM12878	blood:	n/a	n/a
19	CHD1	chr6:25147481-25147774	GM12878	blood:	n/a	n/a
20	CHD2	chr6:25147409-25147799	GM12878	blood:	n/a	n/a
21	CHD2	chr6:25137341-25137374	GM12878	blood:	n/a	n/a
22	CTCF	chr6:25138520-25138670	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr6:25137300-25137450	HCFaa	heart:	n/a	n/a
24	CTCF	chr6:25138480-25138630	GM12872	blood:	n/a	n/a
25	CTCF	chr6:25138532-25138663	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr6:25138487-25138692	NHEK	skin:	n/a	n/a
27	CTCF	chr6:25138480-25138630	HFF	foreskin:	n/a	n/a
28	CTCF	chr6:25138540-25138690	AG09319	gingival:	n/a	n/a
29	CTCF	chr6:25142760-25142910	BE2_C	brain:	n/a	n/a
30	CTCF	chr6:25138500-25138650	GM12874	blood:	n/a	n/a
31	CTCF	chr6:25138500-25138650	GM12873	blood:	n/a	n/a
32	CTCF	chr6:25138540-25138690	BE2_C	brain:	n/a	n/a
33	CTCF	chr6:25138503-25138683	GM19238	blood:	n/a	n/a
34	CTCF	chr6:25138540-25138690	WI-38	lung:	n/a	n/a
35	CTCF	chr6:25138508-25138649	GM12891	blood:	n/a	n/a
36	CTCF	chr6:25138524-25138668	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:25138488-25138705	Gliobla	brain:	n/a	n/a
38	CTCF	chr6:25138505-25138674	ProgFib	skin:	n/a	n/a
39	CTCF	chr6:25138580-25138730	BJ	skin:	n/a	n/a
40	CTCF	chr6:25138440-25138590	GM12872	blood:	n/a	n/a
41	CTCF	chr6:25138567-25138597	GM13977	blood:	n/a	n/a
42	CTCF	chr6:25138480-25138630	GM12864	blood:	n/a	n/a
43	CTCF	chr6:25138500-25138650	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr6:25138400-25138550	WI-38	lung:	n/a	n/a
45	CTCF	chr6:25138380-25138530	RPTEC	kidney:	n/a	n/a
46	CTCF	chr6:25138720-25138870	GM12873	blood:	n/a	n/a
47	CTCF	chr6:25138520-25138670	AG04449	skin:	n/a	n/a
48	CTCF	chr6:25138511-25138666	GM19240	blood:	n/a	n/a
49	CTCF	chr6:25138460-25138610	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr6:25138540-25138690	GM12873	blood:	n/a	n/a

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:25137864-25137914	AG09309	skin:	n/a
2	chr6:25138632-25138682	GM12891	blood:	n/a
3	chr6:25137971-25138021	SK-N-MC	brain:	n/a
4	chr6:25137864-25137914	AG10803	skin:	n/a
5	chr6:25137864-25137914	AG09309	skin:	n/a
6	chr6:25138632-25138682	GM12891	blood:	n/a
7	chr6:25137971-25138021	SK-N-MC	brain:	n/a
8	chr6:25137864-25137914	AG10803	skin:	n/a
9	chr6:25140377-25140427	AG04450	lung:	fetal
10	chr6:25140136-25140186	NH-A	brain:	n/a
11	chr6:25140136-25140186	AG09319	gingival:	n/a
12	chr6:25143214-25143264	RPTEC	kidney:	n/a
13	chr6:25138551-25138601	HEK293	kidney:	embryo
14	chr6:25140136-25140186	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:25140091-25140141	PrEC	prostate:	n/a
16	chr6:25143214-25143264	ECC-1	luminal epithelium:	n/a
17	chr6:25140091-25140141	IMR90	lung:	fetal
18	chr6:25138169-25138219	IMR90	lung:	fetal
19	chr6:25138169-25138219	AoSMC	blood vessel:	n/a
20	chr6:25138951-25139001	HIPEpiC	eye:	n/a
21	chr6:25140377-25140427	HMEC	breast:	n/a
22	chr6:25140091-25140141	HCF	heart:	n/a
23	chr6:25140377-25140427	HAEpiC	amniotic membrane:	n/a
24	chr6:25138632-25138682	NHDF-neo	bronchial:	n/a
25	chr6:25138551-25138601	U87	brain:	n/a
26	chr6:25138905-25138955	AG09319	gingival:	n/a
27	chr6:25140091-25140141	SK-N-MC	brain:	n/a
28	chr6:25140091-25140141	HEK293	kidney:	embryo
29	chr6:25138551-25138601	AG09319	gingival:	n/a
30	chr6:25138169-25138219	SAEC	small airway:	n/a
31	chr6:25138905-25138955	BE2_C	brain:	n/a
32	chr6:25137971-25138021	A549	lung:	n/a
33	chr6:25138632-25138682	AoSMC	blood vessel:	n/a
34	chr6:25137864-25137914	Caco-2	colon:	n/a
35	chr6:25137971-25138021	HRCEpiC	kidney:	n/a
36	chr6:25137864-25137914	HNPCEpiC	eye:	n/a
37	chr6:25138905-25138955	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:25140063-25140113	A549	lung:	n/a
39	chr6:25138169-25138219	SKMC	muscle:	n/a
40	chr6:25138632-25138682	SK-N-SH_RA	brain:	n/a
41	chr6:25138632-25138682	T-47D	breast:	n/a
42	chr6:25138416-25138466	HEEpiC	esophagus:	n/a
43	chr6:25143214-25143264	AG04449	skin:	fetal
44	chr6:25138951-25139001	HRCEpiC	kidney:	n/a
45	chr6:25138905-25138955	Hepatocyte	liver:	n/a
46	chr6:25140136-25140186	GM19239	blood:	n/a
47	chr6:25137864-25137914	MCF-7	breast:	n/a
48	chr6:25138551-25138601	ECC-1	luminal epithelium:	n/a
49	chr6:25138416-25138466	Jurkat	blood:	n/a
50	chr6:25137864-25137914	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:25138546..25140373-chr6:25141189..25143013,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000219682	TF binding region
CMAHP	TF binding region
ENSG00000262400	TF binding region
ENSG00000219682	CpG island
CMAHP	CpG island
ENSG00000262400	CpG island
ENSG00000168405	chromatin interactions
ENSG00000219682	chromatin interactions

Extended variants
information (count: 529 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369316434	chr6:25137021-25137022	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs373045121	chr6:25137084-25137085	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs376248162	chr6:25137093-25137094	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs371381615	chr6:25137109-25137110	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs533394941	chr6:25137135-25137136	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs186555713	chr6:25137144-25137145	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113559050	chr6:25137151-25137152	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs535748576	chr6:25137233-25137234	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs555497949	chr6:25137241-25137242	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs566303815	chr6:25137274-25137275	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs377576384	chr6:25137281-25137282	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs116432071	chr6:25137304-25137305	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141682734	chr6:25137316-25137317	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs375694200	chr6:25137357-25137358	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs545751044	chr6:25137372-25137373	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs303022	chr6:25137401-25137402	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs76647560	chr6:25137418-25137419	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs10547854	chr6:25137434-25137435	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs303021	chr6:25137435-25137436	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs542156607	chr6:25137437-25137438	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs57641455	chr6:25137455-25137456	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs150457904	chr6:25137456-25137457	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs11751334	chr6:25137486-25137487	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs303020	chr6:25137516-25137517	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs71544622	chr6:25137547-25137548	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs70974967	chr6:25137592-25137593	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs527507165	chr6:25137607-25137608	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs541148284	chr6:25137623-25137624	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs368674879	chr6:25137655-25137656	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs564568509	chr6:25137658-25137659	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs79887269	chr6:25137671-25137672	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534259524	chr6:25137705-25137706	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs375519879	chr6:25137733-25137734	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs77746120	chr6:25137746-25137747	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs569722243	chr6:25137777-25137778	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs529534720	chr6:25137871-25137872	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs549312362	chr6:25137872-25137873	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs374520091	chr6:25137936-25137937	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535255314	chr6:25137962-25137963	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs139472856	chr6:25137964-25137965	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs368389965	chr6:25137971-25137972	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs59778363	chr6:25137985-25137986	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs16890134	chr6:25138009-25138010	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs149636829	chr6:25138039-25138040	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs576150339	chr6:25138076-25138077	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs542144421	chr6:25138079-25138080	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs555730569	chr6:25138081-25138082	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs572262943	chr6:25138089-25138090	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs191011351	chr6:25138121-25138122	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs57003751	chr6:25138153-25138154	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:101)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	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	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25116000-25137000	Weak transcription	Lung	lung
2	chr6:25122600-25137000	Weak transcription	Colonic Mucosa	Colon
3	chr6:25122600-25137000	Weak transcription	HSMM	muscle
4	chr6:25122800-25137000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr6:25123800-25138400	Weak transcription	Pancreas	Pancrea
6	chr6:25124400-25138200	Weak transcription	Spleen	Spleen
7	chr6:25133200-25137000	Strong transcription	Fetal Thymus	thymus
8	chr6:25133800-25138000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:25134000-25137200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:25135200-25140200	Active TSS	Right Atrium	heart
11	chr6:25135400-25138200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
12	chr6:25135600-25137000	Weak transcription	Psoas Muscle	Psoas
13	chr6:25135800-25137000	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:25136000-25137200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
15	chr6:25136000-25137600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
16	chr6:25136000-25137800	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr6:25136000-25138800	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr6:25136000-25139800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:25136200-25137000	Enhancers	Primary B cells from peripheral blood	blood
20	chr6:25136200-25137000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr6:25136200-25137400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
22	chr6:25136200-25137400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
23	chr6:25136200-25137400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr6:25136200-25137400	Flanking Active TSS	Stomach Smooth Muscle	stomach
25	chr6:25136200-25139000	Active TSS	Left Ventricle	heart
26	chr6:25136200-25139600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr6:25136200-25139800	Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr6:25136200-25140000	Active TSS	Aorta	Aorta
29	chr6:25136400-25137600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr6:25136400-25138200	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr6:25136400-25139200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr6:25136400-25139400	Active TSS	Brain Hippocampus Middle	brain
33	chr6:25136600-25137000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr6:25136600-25137200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:25136600-25137400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
36	chr6:25136600-25137400	Transcr. at gene 5' and 3'	Thymus	Thymus
37	chr6:25136600-25137800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr6:25136600-25138000	Transcr. at gene 5' and 3'	Dnd41	blood
39	chr6:25136600-25139400	Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr6:25136600-25139600	Active TSS	Duodenum Mucosa	Duodenum
41	chr6:25136600-25140000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:25136800-25137000	Enhancers	Fetal Lung	lung
43	chr6:25136800-25137000	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr6:25136800-25137000	Flanking Active TSS	HSMMtube	muscle
45	chr6:25136800-25137200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:25136800-25137200	Flanking Active TSS	Rectal Smooth Muscle	rectum
47	chr6:25136800-25137400	Enhancers	Primary B cells from cord blood	blood
48	chr6:25136800-25137400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr6:25136800-25137400	Flanking Active TSS	Colon Smooth Muscle	Colon
50	chr6:25136800-25137400	Flanking Active TSS	GM12878-XiMat	blood

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