Variant report

Variant	esv34020
Chromosome Location	chr6:24481299-24606036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2839)
CpG islands
(count:1715)
Chromatin interactive
region (count:149)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2839 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:24504604-24505596	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:24521320-24521362	K562	blood:	n/a	n/a
3	ARID3A	chr6:24495393-24495660	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:24566749-24566949	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:24581382-24581649	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:24493729-24494132	K562	blood:	n/a	chr6:24493902-24493918 chr6:24493901-24493917
7	ATF1	chr6:24538268-24538289	K562	blood:	n/a	n/a
8	ATF1	chr6:24583673-24583987	K562	blood:	n/a	n/a
9	ATF2	chr6:24601156-24601442	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr6:24522483-24523007	GM12878	blood:	n/a	n/a
11	ATF2	chr6:24522471-24523064	GM12878	blood:	n/a	n/a
12	ATF2	chr6:24494940-24495302	GM12878	blood:	n/a	n/a
13	ATF2	chr6:24583571-24583950	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr6:24522654-24523097	GM12878	blood:	n/a	n/a
15	ATF3	chr6:24522744-24522938	K562	blood:	n/a	n/a
16	BACH1	chr6:24521217-24521365	K562	blood:	n/a	n/a
17	BACH1	chr6:24546392-24546606	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:24493772-24494244	K562	blood:	n/a	n/a
19	BACH1	chr6:24494725-24495996	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:24536694-24536695	K562	blood:	n/a	n/a
21	BACH1	chr6:24522747-24522954	K562	blood:	n/a	n/a
22	BACH1	chr6:24492885-24493068	K562	blood:	n/a	n/a
23	BACH1	chr6:24493799-24494036	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:24521218-24521401	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr6:24522644-24523026	GM12878	blood:	n/a	chr6:24522818-24522828 chr6:24522813-24522824
26	BATF	chr6:24554785-24555050	GM12878	blood:	n/a	chr6:24554923-24554934
27	BCL3	chr6:24522589-24522951	GM12878	blood:	n/a	n/a
28	BCLAF1	chr6:24522521-24523081	GM12878	blood:	n/a	n/a
29	BCLAF1	chr6:24494844-24496229	GM12878	blood:	n/a	chr6:24495035-24495044 chr6:24495925-24495934
30	BCLAF1	chr6:24522353-24523202	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:24547467-24547837	K562	blood:	n/a	n/a
32	BHLHE40	chr6:24525096-24525367	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:24492940-24492941	GM12878	blood:	n/a	n/a
34	BHLHE40	chr6:24547501-24547791	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:24583778-24583996	GM12878	blood:	n/a	n/a
36	BHLHE40	chr6:24521227-24521585	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:24522571-24523157	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:24494988-24496151	GM12878	blood:	n/a	n/a
39	BHLHE40	chr6:24522658-24523096	K562	blood:	n/a	n/a
40	BHLHE40	chr6:24494774-24496091	HepG2	liver:	n/a	n/a
41	BHLHE40	chr6:24494635-24496143	K562	blood:	n/a	n/a
42	BRCA1	chr6:24494979-24495107	HepG2	liver:	n/a	n/a
43	BRCA1	chr6:24494941-24495205	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr6:24546481-24546534	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr6:24521404-24521423	HepG2	liver:	n/a	n/a
46	BRCA1	chr6:24495667-24495921	HepG2	liver:	n/a	n/a
47	BRCA1	chr6:24589724-24589913	H1-hESC	embryonic stem cell:	n/a	n/a
48	CBX3	chr6:24494815-24496262	K562	blood:	n/a	n/a
49	CBX3	chr6:24497442-24497839	K562	blood:	n/a	n/a
50	CBX3	chr6:24522646-24523049	K562	blood:	n/a	n/a

(count:1715 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:24495059-24495109	AoSMC	blood vessel:	n/a
2	chr6:24588956-24589006	ovcar-3	ovarian:	n/a
3	chr6:24494462-24494512	RPTEC	kidney:	n/a
4	chr6:24494793-24494843	CMK	blood:	n/a
5	chr6:24545633-24545683	HIPEpiC	eye:	n/a
6	chr6:24489855-24489905	RPTEC	kidney:	n/a
7	chr6:24495059-24495109	PANC-1	pancreas:	n/a
8	chr6:24495059-24495109	AoSMC	blood vessel:	n/a
9	chr6:24588956-24589006	ovcar-3	ovarian:	n/a
10	chr6:24494462-24494512	RPTEC	kidney:	n/a
11	chr6:24494793-24494843	CMK	blood:	n/a
12	chr6:24545633-24545683	HIPEpiC	eye:	n/a
13	chr6:24489855-24489905	RPTEC	kidney:	n/a
14	chr6:24495059-24495109	PANC-1	pancreas:	n/a
15	chr6:24495072-24495122	HL-60	blood:	n/a
16	chr6:24495061-24495111	LNCaP	prostate:	n/a
17	chr6:24495072-24495122	Caco-2	colon:	n/a
18	chr6:24545633-24545683	ECC-1	luminal epithelium:	n/a
19	chr6:24494462-24494512	GM19239	blood:	n/a
20	chr6:24583848-24583898	GM12878	blood:	n/a
21	chr6:24494462-24494512	HRE	kidney:	n/a
22	chr6:24499591-24499641	GM06990	blood:	n/a
23	chr6:24583614-24583664	HNPCEpiC	eye:	n/a
24	chr6:24494605-24494655	SAEC	small airway:	n/a
25	chr6:24486038-24486088	HRPEpiC	eye:	n/a
26	chr6:24583477-24583527	HRCEpiC	kidney:	n/a
27	chr6:24535222-24535272	NB4	blood:	n/a
28	chr6:24491317-24491367	HIPEpiC	eye:	n/a
29	chr6:24583614-24583664	HAEpiC	amniotic membrane:	n/a
30	chr6:24491098-24491148	MCF10A-Er-Src	breast:	n/a
31	chr6:24583477-24583527	MCF10A-Er-Src	breast:	n/a
32	chr6:24583477-24583527	NHDF-neo	bronchial:	n/a
33	chr6:24494793-24494843	SK-N-MC	brain:	n/a
34	chr6:24489770-24489820	MCF10A-Er-Src	breast:	n/a
35	chr6:24494665-24494715	HCT-116	colon:	n/a
36	chr6:24491317-24491367	HAEpiC	amniotic membrane:	n/a
37	chr6:24486038-24486088	AG10803	skin:	n/a
38	chr6:24588956-24589006	HRE	kidney:	n/a
39	chr6:24489887-24489937	AG04449	skin:	fetal
40	chr6:24489770-24489820	CMK	blood:	n/a
41	chr6:24491098-24491148	IMR90	lung:	fetal
42	chr6:24495614-24495664	MCF-7	breast:	n/a
43	chr6:24495264-24495314	HUVEC	blood vessel:	n/a
44	chr6:24545633-24545683	HEK293	kidney:	embryo
45	chr6:24583723-24583773	HRPEpiC	eye:	n/a
46	chr6:24583723-24583773	ovcar-3	ovarian:	n/a
47	chr6:24489887-24489937	GM12892	blood:	n/a
48	chr6:24588956-24589006	AG04450	lung:	fetal
49	chr6:24489770-24489820	NB4	blood:	n/a
50	chr6:24491168-24491218	ProgFib	skin:	n/a

(count:149 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:24497206..24500144-chr6:24502439..24504926,2	MCF-7	breast:
2	chr6:24563668..24565517-chr6:24568197..24570013,2	MCF-7	breast:
3	chr6:24578480..24581116-chr6:24582256..24584782,2	MCF-7	breast:
4	chr6:24574532..24577193-chr6:24720841..24722364,2	MCF-7	breast:
5	chr6:24493986..24495664-chr6:24558273..24561120,2	MCF-7	breast:
6	chr6:24583415..24585210-chr6:24588851..24590739,2	K562	blood:
7	chr6:24473016..24474847-chr6:24495882..24498664,2	K562	blood:
8	chr6:24580785..24582089-chr6:24695048..24696580,9	MCF-7	breast:
9	chr6:24490344..24492283-chr6:24493726..24496491,4	MCF-7	breast:
10	chr6:24493044..24496959-chr6:24499053..24507631,9	MCF-7	breast:
11	chr6:24431084..24431585-chr6:24495592..24496144,2	MCF-7	breast:
12	chr6:24595027..24597717-chr6:24776172..24778423,2	K562	blood:
13	chr6:24431387..24432156-chr6:24520936..24521780,2	K562	blood:
14	chr6:24583515..24584121-chr6:24612514..24613415,2	K562	blood:
15	chr6:24570345..24573148-chr6:24573437..24575149,2	K562	blood:
16	chr6:24495638..24500234-chr6:24504925..24509115,5	K562	blood:
17	chr6:24492633..24493385-chr6:24520875..24521776,3	MCF-7	breast:
18	chr6:24489101..24491684-chr6:24493403..24495493,2	MCF-7	breast:
19	chr6:24524808..24525319-chr6:24581024..24581902,2	MCF-7	breast:
20	chr6:24492475..24493366-chr6:24524815..24525673,2	MCF-7	breast:
21	chr6:24530783..24533712-chr6:24700418..24704307,3	MCF-7	breast:
22	chr6:24479058..24482024-chr6:24719386..24721628,2	MCF-7	breast:
23	chr6:24495638..24500234-chr6:24504925..24509115,5	K562	blood:
24	chr6:24546115..24547618-chr6:24548404..24550635,2	K562	blood:
25	chr6:24580668..24582664-chr6:24719148..24720850,2	K562	blood:
26	chr6:24483355..24485478-chr6:24495554..24497195,2	MCF-7	breast:
27	chr6:24504155..24505791-chr6:24513770..24515648,2	K562	blood:
28	chr6:24492475..24493366-chr6:24524815..24525673,2	MCF-7	breast:
29	chr6:24524047..24526030-chr6:24583848..24585910,2	MCF-7	breast:
30	chr6:24487096..24491354-chr6:24491448..24495730,8	K562	blood:
31	chr6:24544075..24545945-chr6:24559657..24561591,2	MCF-7	breast:
32	chr6:24430350..24432062-chr6:24520550..24521835,7	MCF-7	breast:
33	chr6:24504725..24507769-chr6:24719049..24722072,3	MCF-7	breast:
34	chr6:24581924..24583883-chr6:24690538..24692523,2	MCF-7	breast:
35	chr6:24555919..24558537-chr6:24563270..24565102,2	MCF-7	breast:
36	chr6:24524808..24525319-chr6:24581024..24581902,2	MCF-7	breast:
37	chr6:24593795..24596889-chr6:24599933..24601863,3	K562	blood:
38	chr6:24590802..24593221-chr6:24599918..24601431,2	K562	blood:
39	chr6:24563668..24565517-chr6:24568197..24570013,2	MCF-7	breast:
40	chr6:24495510..24496378-chr6:24695478..24696466,2	MCF-7	breast:
41	chr6:24489101..24491684-chr6:24493403..24495493,2	MCF-7	breast:
42	chr6:24478986..24481425-chr6:24502139..24505080,2	K562	blood:
43	chr6:24402909..24405943-chr6:24492830..24496087,3	K562	blood:
44	chr6:24282882..24283800-chr6:24521072..24521695,2	K562	blood:
45	chr6:24601929..24604741-chr6:24605284..24606848,2	K562	blood:
46	chr6:24492633..24493385-chr6:24520875..24521776,3	MCF-7	breast:
47	chr6:24488265..24492557-chr6:24493494..24498787,7	K562	blood:
48	chr6:24496929..24500234-chr6:24504252..24507783,4	K562	blood:
49	chr6:24586729..24589298-chr6:24716794..24718796,2	K562	blood:
50	chr6:24555919..24558537-chr6:24563270..24565102,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0319-1	chr6:24534020-24535373	NONHSAT108115
2	lnc-KIAA0319-1	chr6:24539164-24539510	NONHSAT108115

No data

Variant related genes	Relation type
ALDH5A1	TF binding region
GPLD1	TF binding region
KRT8P43	TF binding region
ALDH5A1	CpG island
GPLD1	CpG island
KRT8P43	CpG island
ENSG00000111802	chromatin interactions
ENSG00000112294	chromatin interactions
ENSG00000112304	chromatin interactions
ENSG00000112312	chromatin interactions
ENSG00000112293	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000124532	chromatin interactions
ENSG00000272345	chromatin interactions

Extended variants
information (count: 5348 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5348 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2760139	chr6:24481299-24481300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7773122	chr6:24481300-24481301	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs78808915	chr6:24481312-24481313	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
4	rs377631987	chr6:24481320-24481321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs572552090	chr6:24481357-24481358	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2817208	chr6:24481373-24481374	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs546052630	chr6:24481374-24481375	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs114343627	chr6:24481398-24481399	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs114919723	chr6:24481431-24481432	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs542107589	chr6:24481455-24481456	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs144727204	chr6:24481531-24481532	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs13218564	chr6:24481542-24481543	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs547748901	chr6:24481545-24481546	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564457855	chr6:24481555-24481556	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs202235007	chr6:24481566-24481567	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs62400492	chr6:24481569-24481570	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs7773357	chr6:24481570-24481571	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs200361254	chr6:24481572-24481573	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs527301719	chr6:24481573-24481574	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs57649807	chr6:24481586-24481587	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs62400493	chr6:24481590-24481591	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs549982589	chr6:24481613-24481614	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569867166	chr6:24481614-24481615	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs533455662	chr6:24481673-24481674	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543770798	chr6:24481685-24481686	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201501327	chr6:24481748-24481749	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549451405	chr6:24481753-24481754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184596746	chr6:24481756-24481757	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs148542438	chr6:24481769-24481770	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs553710936	chr6:24481812-24481813	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545564480	chr6:24481823-24481824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs140603157	chr6:24481834-24481835	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534717662	chr6:24481837-24481838	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs570575519	chr6:24481862-24481863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2817209	chr6:24481878-24481879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs556405676	chr6:24481883-24481884	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs142772850	chr6:24481900-24481901	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542007146	chr6:24481929-24481930	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7749066	chr6:24481934-24481935	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572289834	chr6:24481935-24481936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs147237179	chr6:24481944-24481945	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs564112892	chr6:24481971-24481972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533253136	chr6:24481980-24481981	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190306938	chr6:24481981-24481982	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367989739	chr6:24481982-24481983	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs563432576	chr6:24481990-24481991	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs529489262	chr6:24481993-24481994	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549529970	chr6:24482152-24482153	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs566275930	chr6:24482182-24482183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs528746625	chr6:24482185-24482186	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Myelodysplastic syndrome	21251322	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
XY gonadal dysgenesis	20685758	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24429000-24494200	Weak transcription	Primary B cells from cord blood	blood
2	chr6:24429400-24483800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:24438400-24483200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:24447400-24490400	Weak transcription	Brain Anterior Caudate	brain
5	chr6:24448800-24488000	Weak transcription	Fetal Muscle Leg	muscle
6	chr6:24458600-24489000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr6:24458800-24492800	Weak transcription	Thymus	Thymus
8	chr6:24458800-24494000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr6:24470400-24483800	Weak transcription	Aorta	Aorta
10	chr6:24470600-24494600	Weak transcription	Left Ventricle	heart
11	chr6:24471800-24481600	Strong transcription	Liver	Liver
12	chr6:24472600-24489400	Weak transcription	HepG2	liver
13	chr6:24473000-24494600	Weak transcription	Ovary	ovary
14	chr6:24479600-24490200	Weak transcription	Hela-S3	cervix
15	chr6:24480400-24493600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:24481600-24484600	Weak transcription	Liver	Liver
17	chr6:24481800-24482000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:24483200-24483800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:24483200-24483800	Enhancers	GM12878-XiMat	blood
20	chr6:24483200-24484800	Weak transcription	Brain Angular Gyrus	brain
21	chr6:24483800-24494000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr6:24484600-24486000	Strong transcription	Liver	Liver
23	chr6:24484800-24485400	Strong transcription	Brain Angular Gyrus	brain
24	chr6:24485200-24485600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:24485200-24485600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr6:24485400-24494000	Weak transcription	Brain Angular Gyrus	brain
27	chr6:24486000-24487200	Weak transcription	Liver	Liver
28	chr6:24487200-24487800	Enhancers	Liver	Liver
29	chr6:24487800-24488400	Flanking Active TSS	Liver	Liver
30	chr6:24488000-24492000	Enhancers	Fetal Muscle Leg	muscle
31	chr6:24488400-24490000	Active TSS	Liver	Liver
32	chr6:24489000-24489400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:24489000-24490000	Enhancers	Fetal Muscle Trunk	muscle
34	chr6:24489000-24490600	Enhancers	Adipose Nuclei	Adipose
35	chr6:24489000-24491600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr6:24489200-24489400	Enhancers	Right Ventricle	heart
37	chr6:24489400-24490200	Weak transcription	Right Ventricle	heart
38	chr6:24489400-24490600	Enhancers	HepG2	liver
39	chr6:24489600-24489800	Enhancers	Right Atrium	heart
40	chr6:24489600-24492000	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr6:24489800-24490000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr6:24489800-24494600	Weak transcription	Right Atrium	heart
43	chr6:24490000-24490400	Flanking Active TSS	Liver	Liver
44	chr6:24490000-24490400	Weak transcription	Fetal Muscle Trunk	muscle
45	chr6:24490200-24490400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr6:24490200-24490400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr6:24490200-24490400	Enhancers	Right Ventricle	heart
48	chr6:24490200-24490600	Enhancers	Colon Smooth Muscle	Colon
49	chr6:24490200-24490600	Enhancers	Hela-S3	cervix
50	chr6:24490200-24490800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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