Variant report

Variant	nsv884536
Chromosome Location	chr6:31947594-32003881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:665)
CpG islands
(count:2263)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31947365-31947781	K562	blood:	n/a	n/a
2	BHLHE40	chr6:32003438-32003784	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:31949559-31949880	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:31982297-31982618	HepG2	liver:	n/a	n/a
5	BHLHE40	chr6:31970701-31971047	HepG2	liver:	n/a	n/a
6	CBX3	chr6:31952793-31953135	K562	blood:	n/a	n/a
7	CBX3	chr6:31952664-31953239	K562	blood:	n/a	n/a
8	CBX3	chr6:32003260-32004138	K562	blood:	n/a	n/a
9	CBX3	chr6:31985535-31985921	K562	blood:	n/a	n/a
10	CBX3	chr6:31970387-31971162	K562	blood:	n/a	n/a
11	CBX3	chr6:31990799-31991208	K562	blood:	n/a	n/a
12	CBX3	chr6:31985480-31985931	K562	blood:	n/a	n/a
13	CBX3	chr6:31982302-31982628	K562	blood:	n/a	n/a
14	CBX3	chr6:31990712-31991199	K562	blood:	n/a	n/a
15	CBX3	chr6:31989858-31990273	K562	blood:	n/a	n/a
16	CBX3	chr6:31970603-31971015	K562	blood:	n/a	n/a
17	CBX3	chr6:31980155-31981063	K562	blood:	n/a	n/a
18	CBX3	chr6:32003387-32003757	K562	blood:	n/a	n/a
19	CBX3	chr6:31965417-31965721	K562	blood:	n/a	n/a
20	CBX3	chr6:31958022-31958441	K562	blood:	n/a	n/a
21	CBX3	chr6:31989920-31990157	K562	blood:	n/a	n/a
22	CBX3	chr6:31957963-31958493	K562	blood:	n/a	n/a
23	CCNT2	chr6:31947256-31947610	K562	blood:	n/a	n/a
24	CEBPB	chr6:31970725-31971176	K562	blood:	n/a	n/a
25	CEBPB	chr6:32003276-32004129	K562	blood:	n/a	n/a
26	CEBPB	chr6:31970574-31971273	K562	blood:	n/a	n/a
27	CEBPB	chr6:32003420-32003920	K562	blood:	n/a	n/a
28	CEBPD	chr6:31972233-31972447	HepG2	liver:	n/a	n/a
29	CEBPD	chr6:31980664-31980987	K562	blood:	n/a	n/a
30	CEBPD	chr6:32003343-32003982	K562	blood:	n/a	n/a
31	CEBPD	chr6:31970600-31971236	K562	blood:	n/a	n/a
32	CTCF	chr6:31957591-31957672	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:31990346-31990445	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:31972800-31972893	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr6:31982918-31982945	GM12878	blood:	n/a	n/a
36	CTCF	chr6:31990314-31990438	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:31957304-31957419	GM13976	blood:	n/a	n/a
38	CTCF	chr6:31957067-31957570	K562	blood:	n/a	n/a
39	CTCF	chr6:31957261-31957387	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:31996871-31996889	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:31982815-31982922	GM20000	blood:	n/a	n/a
42	CTCF	chr6:31975074-31975172	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:31990012-31990158	GM12878	blood:	n/a	n/a
44	CTCF	chr6:31989982-31990151	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:31957348-31957448	GM10266	blood:	n/a	n/a
46	CTCF	chr6:31964080-31964162	HepG2	liver:	n/a	chr6:31964112-31964133 chr6:31964119-31964132 chr6:31964117-31964135
47	CTCF	chr6:31985548-31985578	GM20000	blood:	n/a	n/a
48	CTCF	chr6:31964090-31964119	GM12891	blood:	n/a	n/a
49	CTCF	chr6:31989994-31990170	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:31957279-31957346	GM12891	blood:	n/a	n/a

(count:2263 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31964288-31964338	BE2_C	brain:	n/a
2	chr6:31978789-31978839	PFSK-1	brain:	n/a
3	chr6:31964391-31964441	PANC-1	pancreas:	n/a
4	chr6:31980856-31980906	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:31973051-31973101	HEEpiC	esophagus:	n/a
6	chr6:31963892-31963942	A549	lung:	n/a
7	chr6:31964288-31964338	BE2_C	brain:	n/a
8	chr6:31978789-31978839	PFSK-1	brain:	n/a
9	chr6:31964391-31964441	PANC-1	pancreas:	n/a
10	chr6:31980856-31980906	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:31973051-31973101	HEEpiC	esophagus:	n/a
12	chr6:31963892-31963942	A549	lung:	n/a
13	chr6:31973051-31973101	Jurkat	blood:	n/a
14	chr6:31980856-31980906	HL-60	blood:	n/a
15	chr6:31964315-31964365	A549	lung:	n/a
16	chr6:31963919-31963969	HUVEC	blood vessel:	n/a
17	chr6:31997026-31997076	IMR90	lung:	fetal
18	chr6:31980836-31980886	HAEpiC	amniotic membrane:	n/a
19	chr6:31980845-31980895	HL-60	blood:	n/a
20	chr6:31964315-31964365	IMR90	lung:	fetal
21	chr6:31977506-31977556	MCF10A-Er-Src	breast:	n/a
22	chr6:31964754-31964804	NHBE	bronchial:	n/a
23	chr6:31963526-31963576	LNCaP	prostate:	n/a
24	chr6:31964274-31964324	GM12878	blood:	n/a
25	chr6:31980845-31980895	Hela-S3	cervix:	n/a
26	chr6:31977443-31977493	SK-N-SH	brain:	n/a
27	chr6:31964274-31964324	HUVEC	blood vessel:	n/a
28	chr6:31964315-31964365	HAEpiC	amniotic membrane:	n/a
29	chr6:31980046-31980096	HUVEC	blood vessel:	n/a
30	chr6:31997059-31997109	ECC-1	luminal epithelium:	n/a
31	chr6:31976687-31976737	PANC-1	pancreas:	n/a
32	chr6:31980046-31980096	ProgFib	skin:	n/a
33	chr6:31977443-31977493	GM12878	blood:	n/a
34	chr6:31964193-31964243	HUVEC	blood vessel:	n/a
35	chr6:31963526-31963576	HNPCEpiC	eye:	n/a
36	chr6:31963919-31963969	Hela-S3	cervix:	n/a
37	chr6:31973345-31973395	NT2-D1	testis:	n/a
38	chr6:31997491-31997541	AoSMC	blood vessel:	n/a
39	chr6:31973180-31973230	H1-hESC	embryonic stem cell:	embryo
40	chr6:31963526-31963576	IMR90	lung:	fetal
41	chr6:31980856-31980906	PANC-1	pancreas:	n/a
42	chr6:31977599-31977649	GM12878	blood:	n/a
43	chr6:31997026-31997076	AoSMC	blood vessel:	n/a
44	chr6:31977599-31977649	HL-60	blood:	n/a
45	chr6:31963892-31963942	SK-N-MC	brain:	n/a
46	chr6:31974906-31974956	AG10803	skin:	n/a
47	chr6:31963919-31963969	NHBE	bronchial:	n/a
48	chr6:31976720-31976770	BJ	skin:	n/a
49	chr6:31963912-31963962	PrEC	prostate:	n/a
50	chr6:31963892-31963942	NH-A	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31868623..31870778-chr6:31945874..31948322,2	K562	blood:
2	chr6:31912743..31916758-chr6:31944927..31949257,3	K562	blood:
3	chr6:31938987..31942159-chr6:31944563..31949146,6	MCF-7	breast:
4	chr6:31935647..31937211-chr6:31946410..31948036,2	K562	blood:
5	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOM3Z-2	chr6:31970797-31971298	ENSG00000233627.2
2	lnc-DOM3Z-2	chr6:31967753-31969345	ENSG00000233627.2
3	lnc-TNXB-6	chr6:32000490-32002082	ENSG00000229776.1
4	lnc-TNXB-6	chr6:32003534-32004035	ENSG00000229776.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	STK19	hsa-miR-29c-3p	chr6:31981823-31981843
2	STK19	hsa-miR-29c-3p	chr6:31949085-31949105

Variant related genes	Relation type
TNXA	TF binding region
STK19P	TF binding region
CYP21A2	TF binding region
STK19	TF binding region
CYP21A1P	TF binding region
ENSG00000268923	TF binding region
C4A-AS1	TF binding region
C4A	TF binding region
C4B	TF binding region
TNXA	CpG island
STK19P	CpG island
CYP21A2	CpG island
STK19	CpG island
CYP21A1P	CpG island
ENSG00000268923	CpG island
C4A-AS1	CpG island
C4A	CpG island
C4B	CpG island
ENSG00000204351	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000243649	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000204344	chromatin interactions

Extended variants
information (count: 685 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs389512	chr6:31947594-31947595	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551245949	chr6:31947634-31947635	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs573578869	chr6:31947652-31947653	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs368999420	chr6:31947683-31947684	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs147233808	chr6:31947692-31947693	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs562280820	chr6:31947706-31947707	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs574554664	chr6:31947748-31947749	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs116196017	chr6:31947804-31947805	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs377573133	chr6:31947890-31947891	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs533783241	chr6:31947901-31947902	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs114632474	chr6:31947917-31947918	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs551482064	chr6:31948006-31948007	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs530467043	chr6:31948016-31948017	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs118178906	chr6:31948022-31948023	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs6904886	chr6:31948029-31948030	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs563992443	chr6:31948060-31948061	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs140857097	chr6:31948091-31948092	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs9391732	chr6:31948097-31948098	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs190486403	chr6:31948107-31948108	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs533747654	chr6:31948131-31948132	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs182148351	chr6:31948155-31948156	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs569231522	chr6:31948201-31948202	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs376107079	chr6:31948202-31948203	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs558139309	chr6:31948217-31948218	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs369081587	chr6:31948226-31948227	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs573540461	chr6:31948255-31948256	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs373414495	chr6:31948256-31948257	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs534517982	chr6:31948260-31948261	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs151183324	chr6:31948272-31948273	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs140503088	chr6:31948275-31948276	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs267600972	chr6:31948278-31948279	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs200696149	chr6:31948311-31948312	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs28441225	chr6:31948400-31948401	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs200620398	chr6:31948422-31948423	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs70990293	chr6:31948425-31948426	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201442394	chr6:31948433-31948434	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs371041447	chr6:31948452-31948453	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs142791776	chr6:31948473-31948474	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs41267122	chr6:31948474-31948475	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs201134143	chr6:31948502-31948503	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs561534965	chr6:31948507-31948508	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs529123063	chr6:31948524-31948525	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs550753928	chr6:31948533-31948534	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569210209	chr6:31948542-31948543	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs533482344	chr6:31948557-31948558	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs551457703	chr6:31948635-31948636	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs566899533	chr6:31948640-31948641	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534481779	chr6:31948659-31948660	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556137098	chr6:31948715-31948716	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs56337326	chr6:31949352-31949353	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31941000-31947600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:31941000-31949600	Weak transcription	Right Ventricle	heart
3	chr6:31941000-31949800	Weak transcription	Gastric	stomach
4	chr6:31941200-31949200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr6:31941200-31949400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:31941200-31949400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:31941200-31950000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr6:31941400-31947600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:31941400-31949000	Weak transcription	Colonic Mucosa	Colon
10	chr6:31941400-31949400	Weak transcription	Primary B cells from cord blood	blood
11	chr6:31941400-31949400	Weak transcription	NH-A	brain
12	chr6:31941400-31950000	Weak transcription	Fetal Kidney	kidney
13	chr6:31941600-31947600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:31941600-31947600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr6:31941600-31947800	Weak transcription	Fetal Lung	lung
16	chr6:31941600-31948000	Weak transcription	Hela-S3	cervix
17	chr6:31941600-31949200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:31941600-31949200	Weak transcription	Colon Smooth Muscle	Colon
19	chr6:31941600-31950000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr6:31941800-31948600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr6:31941800-31950000	Weak transcription	Dnd41	blood
22	chr6:31944800-31948400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:31945400-31948400	Strong transcription	Fetal Muscle Leg	muscle
24	chr6:31945800-31947800	Enhancers	Primary T cells from cord blood	blood
25	chr6:31945800-31947800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr6:31945800-31948400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr6:31945800-31948400	Strong transcription	Fetal Brain Female	brain
28	chr6:31946000-31947800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr6:31946000-31947800	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr6:31946000-31948200	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr6:31946000-31948200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:31946400-31948200	Strong transcription	Placenta	Placenta
33	chr6:31946400-31948400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:31946400-31948400	Strong transcription	Brain Germinal Matrix	brain
35	chr6:31946400-31948400	Strong transcription	Brain Hippocampus Middle	brain
36	chr6:31946400-31948400	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr6:31946400-31948400	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr6:31946600-31947800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:31946600-31948200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:31946600-31948200	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr6:31946600-31948400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr6:31946600-31948400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:31946600-31948400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:31946600-31948400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:31946600-31948400	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr6:31946600-31948400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:31946600-31948400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:31946600-31948400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr6:31946600-31948400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr6:31946600-31948400	Strong transcription	Fetal Intestine Large	intestine

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