Variant report

Variant	nsv1031707
Chromosome Location	chr6:106803325-106896650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1235)
CpG islands
(count:549)
Chromatin interactive
region (count:65)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1235 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:106894067-106894548	HepG2	liver:	n/a	n/a
2	ATF2	chr6:106892765-106893102	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr6:106808147-106808653	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr6:106808344-106808601	HepG2	liver:	n/a	n/a
5	BACH1	chr6:106808167-106808186	K562	blood:	n/a	n/a
6	BACH1	chr6:106809154-106809304	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:106808003-106808919	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:106892804-106893114	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr6:106817696-106817877	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:106808288-106808575	K562	blood:	n/a	n/a
11	BRCA1	chr6:106809158-106809188	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr6:106808313-106808549	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr6:106820744-106821523	HCT-116	colon:	n/a	n/a
14	CBX3	chr6:106807903-106808956	HCT-116	colon:	n/a	n/a
15	CCNT2	chr6:106851313-106851513	K562	blood:	n/a	n/a
16	CCNT2	chr6:106808227-106808739	K562	blood:	n/a	chr6:106808659-106808668
17	CEBPB	chr6:106844970-106845156	IMR90	lung:	n/a	chr6:106845074-106845085
18	CEBPB	chr6:106892807-106893129	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:106859713-106859913	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:106892529-106893153	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:106870390-106870673	IMR90	lung:	n/a	chr6:106870535-106870548 chr6:106870535-106870546
22	CEBPB	chr6:106870379-106870716	HepG2	liver:	n/a	chr6:106870535-106870548 chr6:106870535-106870546
23	CEBPB	chr6:106892731-106893135	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:106808021-106808594	H1-hESC	embryonic stem cell:	n/a	chr6:106808139-106808152
25	CEBPB	chr6:106892791-106893139	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:106870383-106870757	Hela-S3	cervix:	n/a	chr6:106870535-106870548 chr6:106870535-106870546
27	CEBPB	chr6:106866575-106866604	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:106844871-106845163	A549	lung:	n/a	chr6:106845074-106845085
29	CEBPB	chr6:106892790-106893105	K562	blood:	n/a	n/a
30	CEBPB	chr6:106828077-106828081	A549	lung:	n/a	n/a
31	CEBPB	chr6:106820758-106821550	HCT-116	colon:	n/a	n/a
32	CEBPB	chr6:106892802-106893143	A549	lung:	n/a	n/a
33	CEBPB	chr6:106844375-106844652	MCF-7	breast:	n/a	n/a
34	CEBPB	chr6:106870441-106870709	A549	lung:	n/a	chr6:106870535-106870548 chr6:106870535-106870546
35	CEBPB	chr6:106892785-106893218	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:106887260-106887717	MCF-7	breast:	n/a	n/a
37	CEBPB	chr6:106864189-106864617	MCF-7	breast:	n/a	n/a
38	CEBPB	chr6:106856408-106856602	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr6:106889985-106890229	Hela-S3	cervix:	n/a	chr6:106890063-106890074
40	CEBPB	chr6:106820903-106821465	HCT-116	colon:	n/a	n/a
41	CEBPB	chr6:106844959-106845187	HepG2	liver:	n/a	chr6:106845074-106845085
42	CEBPB	chr6:106864304-106864579	MCF-7	breast:	n/a	n/a
43	CHD1	chr6:106807809-106808374	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr6:106808222-106808711	H1-hESC	embryonic stem cell:	n/a	chr6:106808691-106808701
45	CHD2	chr6:106859762-106860077	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr6:106808099-106808191	K562	blood:	n/a	n/a
47	CHD2	chr6:106808300-106808354	HepG2	liver:	n/a	n/a
48	CREB1	chr6:106808285-106808610	A549	lung:	n/a	n/a
49	CREB1	chr6:106808197-106808607	ECC-1	luminal epithelium:	n/a	n/a
50	CTBP2	chr6:106808131-106809411	H1-hESC	embryonic stem cell:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:106808816-106808866	HRE	kidney:	n/a
2	chr6:106819052-106819102	NB4	blood:	n/a
3	chr6:106868843-106868893	HAEpiC	amniotic membrane:	n/a
4	chr6:106804977-106805027	AG10803	skin:	n/a
5	chr6:106808703-106808753	AoSMC	blood vessel:	n/a
6	chr6:106812783-106812833	NB4	blood:	n/a
7	chr6:106809170-106809220	MCF10A-Er-Src	breast:	n/a
8	chr6:106809237-106809287	AG04449	skin:	fetal
9	chr6:106809170-106809220	SK-N-MC	brain:	n/a
10	chr6:106804977-106805027	HIPEpiC	eye:	n/a
11	chr6:106808110-106808160	ProgFib	skin:	n/a
12	chr6:106808816-106808866	K562	blood:	n/a
13	chr6:106808110-106808160	Jurkat	blood:	n/a
14	chr6:106812783-106812833	NHBE	bronchial:	n/a
15	chr6:106808110-106808160	LNCaP	prostate:	n/a
16	chr6:106809237-106809287	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:106808816-106808866	NT2-D1	testis:	n/a
18	chr6:106809170-106809220	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:106809237-106809287	PFSK-1	brain:	n/a
20	chr6:106809237-106809287	IMR90	lung:	fetal
21	chr6:106819052-106819102	RPTEC	kidney:	n/a
22	chr6:106808703-106808753	GM06990	blood:	n/a
23	chr6:106809237-106809287	BJ	skin:	n/a
24	chr6:106808110-106808160	IMR90	lung:	fetal
25	chr6:106819052-106819102	IMR90	lung:	fetal
26	chr6:106808816-106808866	ECC-1	luminal epithelium:	n/a
27	chr6:106804977-106805027	GM19239	blood:	n/a
28	chr6:106808703-106808753	HCT-116	colon:	n/a
29	chr6:106868843-106868893	MCF-7	breast:	n/a
30	chr6:106808703-106808753	A549	lung:	n/a
31	chr6:106808703-106808753	MCF-7	breast:	n/a
32	chr6:106868843-106868893	HCT-116	colon:	n/a
33	chr6:106804977-106805027	HL-60	blood:	n/a
34	chr6:106812783-106812833	NT2-D1	testis:	n/a
35	chr6:106808816-106808866	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:106808816-106808866	HCF	heart:	n/a
37	chr6:106804977-106805027	HCF	heart:	n/a
38	chr6:106868843-106868893	NT2-D1	testis:	n/a
39	chr6:106808703-106808753	HEK293	kidney:	embryo
40	chr6:106809170-106809220	BJ	skin:	n/a
41	chr6:106808110-106808160	SK-N-SH	brain:	n/a
42	chr6:106809170-106809220	Hepatocyte	liver:	n/a
43	chr6:106804977-106805027	NHDF-neo	bronchial:	n/a
44	chr6:106819052-106819102	AG10803	skin:	n/a
45	chr6:106809170-106809220	ovcar-3	ovarian:	n/a
46	chr6:106819052-106819102	HRCEpiC	kidney:	n/a
47	chr6:106808110-106808160	HCM	heart:	n/a
48	chr6:106804977-106805027	NHBE	bronchial:	n/a
49	chr6:106808703-106808753	RPTEC	kidney:	n/a
50	chr6:106808703-106808753	CMK	blood:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:106807999..106808515-chr6:106892101..106893044,2	MCF-7	breast:
2	chr6:106808965..106810935-chr6:106838431..106840040,2	MCF-7	breast:
3	chr6:106808617..106811340-chr6:106821545..106823616,2	MCF-7	breast:
4	chr6:106893943..106894830-chr6:107003943..107005243,5	MCF-7	breast:
5	chr6:106807932..106809126-chr6:106892501..106893325,3	MCF-7	breast:
6	chr6:106894306..106894922-chr6:107318531..107319078,2	K562	blood:
7	chr19:15039996..15040603-chr6:106892565..106893251,2	MCF-7	breast:
8	chr6:106786932..106787612-chr6:106892577..106893519,3	MCF-7	breast:
9	chr6:106782985..106783505-chr6:106892625..106893417,2	K562	blood:
10	chr6:106887436..106888995-chr6:106894077..106896594,2	K562	blood:
11	chr6:106860820..106863674-chr6:106869273..106872080,2	MCF-7	breast:
12	chr6:106842514..106845297-chr6:106886526..106889026,2	MCF-7	breast:
13	chr6:106861901..106864132-chr6:106865487..106868992,4	K562	blood:
14	chr3:64008693..64009614-chr6:106807869..106808706,2	MCF-7	breast:
15	chr6:106847263..106848780-chr6:107352061..107354720,2	MCF-7	breast:
16	chr6:106807797..106809564-chr6:106892316..106894790,2	MCF-7	breast:
17	chr6:106775261..106777423-chr6:106891472..106893784,2	MCF-7	breast:
18	chr6:105932781..105933301-chr6:106807922..106808689,2	K562	blood:
19	chr6:106831242..106833067-chr6:106837715..106840432,2	K562	blood:
20	chr6:106810826..106813749-chr6:106814057..106816280,2	MCF-7	breast:
21	chr6:106829670..106831474-chr6:106841458..106844006,2	MCF-7	breast:
22	chr6:106770748..106773743-chr6:106892839..106894795,2	MCF-7	breast:
23	chr6:106842514..106845297-chr6:106886526..106889026,2	MCF-7	breast:
24	chr6:106807999..106808515-chr6:106892101..106893044,2	MCF-7	breast:
25	chr6:106831567..106833173-chr6:106837715..106840535,2	K562	blood:
26	chr6:106819657..106821574-chr6:106823902..106826523,2	MCF-7	breast:
27	chr6:106860820..106863674-chr6:106869273..106872080,2	MCF-7	breast:
28	chr6:106793639..106796605-chr6:106892288..106895627,3	MCF-7	breast:
29	chr6:106807586..106809435-chr6:106889467..106891139,2	MCF-7	breast:
30	chr6:106831242..106833067-chr6:106837715..106840432,2	K562	blood:
31	chr6:106893993..106894791-chr6:107013993..107015233,6	K562	blood:
32	chr17:59651944..59652826-chr6:106843888..106844454,2	MCF-7	breast:
33	chr6:106803465..106806035-chr6:106806696..106809673,3	K562	blood:
34	chr6:106788817..106792867-chr6:106807861..106810730,3	MCF-7	breast:
35	chr6:106808617..106811340-chr6:106821545..106823616,2	MCF-7	breast:
36	chr6:106807932..106809126-chr6:106892501..106893325,3	MCF-7	breast:
37	chr6:106892627..106893526-chr6:107014079..107015028,6	K562	blood:
38	chr6:106806608..106808537-chr6:106892921..106895314,2	MCF-7	breast:
39	chr6:106858650..106860928-chr6:106870754..106873020,2	K562	blood:
40	chr6:106891526..106894302-chr6:106895961..106897783,2	K562	blood:
41	chr6:106858650..106860928-chr6:106870754..106873020,2	K562	blood:
42	chr6:106806640..106811296-chr6:106885915..106890564,7	MCF-7	breast:
43	chr6:106819657..106821574-chr6:106823902..106826523,2	MCF-7	breast:
44	chr6:106891408..106894325-chr6:107016587..107019305,2	MCF-7	breast:
45	chr6:106884945..106886506-chr6:106958785..106960709,2	MCF-7	breast:
46	chr6:106887436..106888995-chr6:106894077..106896594,2	K562	blood:
47	chr6:106892479..106893508-chr6:107003919..107004825,3	MCF-7	breast:
48	chr6:106893452..106894012-chr6:106997057..106997774,2	MCF-7	breast:
49	chr6:106807797..106809564-chr6:106892316..106894790,2	MCF-7	breast:
50	chr6:26041847..26044156-chr6:106843655..106845155,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG5-3	chr6:106884469-106884815	NONHSAT114235
2	lnc-ATG5-3	chr6:106872036-106872078	NONHSAT114235
3	lnc-ATG5-3	chr6:106872089-106872178	NONHSAT114235

No data

Variant related genes	Relation type
ENSG00000233941	TF binding region
ENSG00000207499	TF binding region
RNA5SP211	TF binding region
ENSG00000233941	CpG island
ENSG00000207499	CpG island
RNA5SP211	CpG island
ENSG00000233941	chromatin interactions
ENSG00000207499	chromatin interactions
ENSG00000196226	chromatin interactions
ENSG00000112297	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000202386	chromatin interactions
ENSG00000057663	chromatin interactions

Extended variants
information (count: 3722 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:3722 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs503518	chr6:106803325-106803326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529124525	chr6:106803345-106803346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189876548	chr6:106803353-106803354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565868132	chr6:106803354-106803355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372965234	chr6:106803381-106803382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34974947	chr6:106803403-106803404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs550984128	chr6:106803451-106803452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117448803	chr6:106803505-106803506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536755622	chr6:106803506-106803507	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556816945	chr6:106803563-106803564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567350345	chr6:106803588-106803589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556754381	chr6:106803592-106803593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs593310	chr6:106803602-106803603	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs573604886	chr6:106803616-106803617	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114644510	chr6:106803619-106803620	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192882749	chr6:106803620-106803621	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs116797337	chr6:106803780-106803781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188768303	chr6:106803785-106803786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544615967	chr6:106803813-106803814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146373095	chr6:106803816-106803817	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs139343754	chr6:106803872-106803873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34890350	chr6:106803967-106803968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150013534	chr6:106803998-106803999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78739867	chr6:106804025-106804026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs528373387	chr6:106804070-106804071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185466031	chr6:106804100-106804101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189374527	chr6:106804128-106804129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145225362	chr6:106804129-106804130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550527687	chr6:106804130-106804131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs11384064	chr6:106804140-106804141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs398110523	chr6:106804141-106804142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567266863	chr6:106804155-106804156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111693686	chr6:106804164-106804165	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546884027	chr6:106804181-106804182	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149138773	chr6:106804195-106804196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539227359	chr6:106804269-106804270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs182020162	chr6:106804330-106804331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575986600	chr6:106804335-106804336	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs590115	chr6:106804339-106804340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs554913951	chr6:106804353-106804354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs472824	chr6:106804363-106804364	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs144012629	chr6:106804368-106804369	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559289518	chr6:106804397-106804398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572739822	chr6:106804428-106804429	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186476986	chr6:106804436-106804437	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12174878	chr6:106804520-106804521	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs530684609	chr6:106804556-106804557	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550330374	chr6:106804658-106804659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560896212	chr6:106804681-106804682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374922083	chr6:106804730-106804731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:920 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106791000-106808200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:106803000-106807800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:106804200-106805000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:106804400-106804600	Bivalent Enhancer	Small Intestine	intestine
5	chr6:106804400-106804600	Bivalent Enhancer	Stomach Mucosa	stomach
6	chr6:106804600-106805000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:106804800-106805200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr6:106805000-106807800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:106805000-106807800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:106805200-106807800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr6:106807600-106807800	Bivalent Enhancer	HepG2	liver
12	chr6:106807800-106808000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
13	chr6:106807800-106808000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr6:106807800-106808000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr6:106807800-106808000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:106807800-106808000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:106807800-106808000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:106807800-106808000	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
19	chr6:106807800-106808000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
20	chr6:106807800-106808000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
21	chr6:106807800-106808000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:106807800-106808000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:106807800-106808000	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
24	chr6:106807800-106808000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:106807800-106808000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:106807800-106808000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:106807800-106808000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
28	chr6:106807800-106808000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
29	chr6:106807800-106808000	Bivalent Enhancer	Colon Smooth Muscle	Colon
30	chr6:106807800-106808000	Bivalent Enhancer	Fetal Intestine Small	intestine
31	chr6:106807800-106808000	Bivalent Enhancer	Fetal Kidney	kidney
32	chr6:106807800-106808000	Enhancers	Pancreas	Pancrea
33	chr6:106807800-106808000	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr6:106807800-106808000	Enhancers	Hela-S3	cervix
35	chr6:106807800-106808000	Enhancers	HMEC	breast
36	chr6:106807800-106808000	Bivalent Enhancer	NHDF-Ad	bronchial
37	chr6:106807800-106808000	Enhancers	NHEK	skin
38	chr6:106807800-106808200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr6:106807800-106808200	Bivalent Enhancer	Primary B cells from cord blood	blood
40	chr6:106807800-106808200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
41	chr6:106807800-106808200	Bivalent Enhancer	Primary T cells from cord blood	blood
42	chr6:106807800-106808200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
43	chr6:106807800-106808200	Flanking Bivalent TSS/Enh	HepG2	liver
44	chr6:106807800-106808400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
45	chr6:106807800-106808400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr6:106807800-106808400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
47	chr6:106807800-106808600	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr6:106807800-106808800	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr6:106807800-106808800	Active TSS	A549	lung
50	chr6:106807800-106809400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum

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