Variant report

Variant	nsv1033646
Chromosome Location	chr6:31328826-31365869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1149)
CpG islands
(count:427)
Chromatin interactive
region (count:31)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31364722-31364990	HepG2	liver:	n/a	n/a
2	ATF1	chr6:31363664-31363872	K562	blood:	n/a	n/a
3	ATF1	chr6:31334724-31334995	K562	blood:	n/a	n/a
4	ATF2	chr6:31334664-31335022	GM12878	blood:	n/a	n/a
5	ATF2	chr6:31334516-31335091	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:31334685-31334994	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:31334694-31334977	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:31365680-31365917	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr6:31334586-31335058	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:31364697-31365042	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:31363629-31364109	K562	blood:	n/a	chr6:31363900-31363913 chr6:31363902-31363911 chr6:31363902-31363911 chr6:31363896-31363917 chr6:31363901-31363910
12	BHLHE40	chr6:31364721-31364947	K562	blood:	n/a	n/a
13	BHLHE40	chr6:31364743-31364948	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:31334679-31335011	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:31334682-31335021	K562	blood:	n/a	n/a
16	BRCA1	chr6:31334661-31335016	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr6:31334769-31334999	GM12878	blood:	n/a	n/a
18	BRCA1	chr6:31334696-31334942	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr6:31334683-31334882	HepG2	liver:	n/a	n/a
20	CBX3	chr6:31334488-31335041	K562	blood:	n/a	n/a
21	CBX3	chr6:31356778-31357202	K562	blood:	n/a	n/a
22	CBX3	chr6:31363551-31364030	K562	blood:	n/a	n/a
23	CCNT2	chr6:31363683-31363925	K562	blood:	n/a	n/a
24	CEBPB	chr6:31334538-31334970	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:31364595-31364963	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:31356057-31356134	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:31334460-31334873	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:31350953-31351272	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:31350988-31351263	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr6:31350946-31351230	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:31334528-31335030	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr6:31346094-31346379	HepG2	liver:	n/a	n/a
33	CEBPD	chr6:31363671-31364078	K562	blood:	n/a	n/a
34	CHD2	chr6:31334798-31334912	K562	blood:	n/a	n/a
35	CHD2	chr6:31334692-31335000	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:31334735-31335043	GM12878	blood:	n/a	n/a
37	CHD2	chr6:31334751-31334971	HepG2	liver:	n/a	n/a
38	CHD2	chr6:31334677-31335021	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr6:31334621-31335037	A549	lung:	n/a	n/a
40	CTCF	chr6:31356780-31356930	RPTEC	kidney:	n/a	n/a
41	CTCF	chr6:31335089-31335202	A549	lung:	n/a	chr6:31335144-31335157 chr6:31335141-31335159
42	CTCF	chr6:31342025-31342188	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:31364711-31365035	GM12878	blood:	n/a	chr6:31364873-31364891 chr6:31364877-31364884 chr6:31364875-31364896
44	CTCF	chr6:31364820-31364970	WERI-Rb-1	eye:	n/a	chr6:31364873-31364891 chr6:31364877-31364884 chr6:31364875-31364896
45	CTCF	chr6:31334726-31334967	ECC-1	luminal epithelium:	n/a	chr6:31334843-31334856 chr6:31334841-31334859 chr6:31334843-31334856 chr6:31334847-31334856 chr6:31334836-31334857 chr6:31334844-31334854 chr6:31334842-31334858
46	CTCF	chr6:31342060-31342210	AG09309	skin:	n/a	n/a
47	CTCF	chr6:31334620-31335035	K562	blood:	n/a	chr6:31334843-31334856 chr6:31334841-31334859 chr6:31334843-31334856 chr6:31334847-31334856 chr6:31334836-31334857 chr6:31334844-31334854 chr6:31334842-31334858
48	CTCF	chr6:31356862-31357156	Hela-S3	cervix:	n/a	chr6:31356989-31357005
49	CTCF	chr6:31356740-31356890	GM12867	blood:	n/a	n/a
50	CTCF	chr6:31334780-31334930	GM12875	blood:	n/a	chr6:31334843-31334856 chr6:31334841-31334859 chr6:31334843-31334856 chr6:31334847-31334856 chr6:31334836-31334857 chr6:31334844-31334854 chr6:31334842-31334858

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31334836-31334886	AG04450	lung:	fetal
2	chr6:31347802-31347852	HNPCEpiC	eye:	n/a
3	chr6:31364902-31364952	ECC-1	luminal epithelium:	n/a
4	chr6:31364895-31364945	SK-N-MC	brain:	n/a
5	chr6:31347802-31347852	AG10803	skin:	n/a
6	chr6:31334738-31334788	HRCEpiC	kidney:	n/a
7	chr6:31347802-31347852	SK-N-MC	brain:	n/a
8	chr6:31364895-31364945	ECC-1	luminal epithelium:	n/a
9	chr6:31364895-31364945	SKMC	muscle:	n/a
10	chr6:31364942-31364992	AG09309	skin:	n/a
11	chr6:31334738-31334788	HCT-116	colon:	n/a
12	chr6:31334738-31334788	HCM	heart:	n/a
13	chr6:31364999-31365049	T-47D	breast:	n/a
14	chr6:31364942-31364992	SK-N-MC	brain:	n/a
15	chr6:31334836-31334886	HRCEpiC	kidney:	n/a
16	chr6:31334738-31334788	BE2_C	brain:	n/a
17	chr6:31347802-31347852	A549	lung:	n/a
18	chr6:31364895-31364945	HAEpiC	amniotic membrane:	n/a
19	chr6:31364902-31364952	HRCEpiC	kidney:	n/a
20	chr6:31364942-31364992	CMK	blood:	n/a
21	chr6:31347802-31347852	NB4	blood:	n/a
22	chr6:31364902-31364952	HEK293	kidney:	embryo
23	chr6:31334836-31334886	PFSK-1	brain:	n/a
24	chr6:31364902-31364952	NHDF-neo	bronchial:	n/a
25	chr6:31364895-31364945	NHDF-neo	bronchial:	n/a
26	chr6:31364999-31365049	BJ	skin:	n/a
27	chr6:31364942-31364992	HCPEpiC	choroid plexus:	n/a
28	chr6:31364942-31364992	AG09319	gingival:	n/a
29	chr6:31364942-31364992	HUVEC	blood vessel:	n/a
30	chr6:31364895-31364945	GM19239	blood:	n/a
31	chr6:31364999-31365049	PANC-1	pancreas:	n/a
32	chr6:31364895-31364945	H1-hESC	embryonic stem cell:	embryo
33	chr6:31347802-31347852	HUVEC	blood vessel:	n/a
34	chr6:31347802-31347852	K562	blood:	n/a
35	chr6:31334738-31334788	RPTEC	kidney:	n/a
36	chr6:31334836-31334886	PANC-1	pancreas:	n/a
37	chr6:31364999-31365049	HCT-116	colon:	n/a
38	chr6:31364902-31364952	SKMC	muscle:	n/a
39	chr6:31364999-31365049	K562	blood:	n/a
40	chr6:31364895-31364945	Caco-2	colon:	n/a
41	chr6:31334738-31334788	T-47D	breast:	n/a
42	chr6:31364902-31364952	HMEC	breast:	n/a
43	chr6:31364942-31364992	Hela-S3	cervix:	n/a
44	chr6:31364895-31364945	HUVEC	blood vessel:	n/a
45	chr6:31334836-31334886	SKMC	muscle:	n/a
46	chr6:31347802-31347852	LNCaP	prostate:	n/a
47	chr6:31347802-31347852	NHBE	bronchial:	n/a
48	chr6:31334738-31334788	K562	blood:	n/a
49	chr6:31334738-31334788	AG04449	skin:	fetal
50	chr6:31364999-31365049	NT2-D1	testis:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31343886..31345657-chr6:31346957..31349841,2	MCF-7	breast:
2	chr6:31164428..31165295-chr6:31333347..31334316,2	MCF-7	breast:
3	chr6:31195002..31197168-chr6:31331435..31333390,2	K562	blood:
4	chr6:31104961..31105839-chr6:31334399..31335415,6	K562	blood:
5	chr6:31364332..31365182-chr6:31410773..31411326,2	MCF-7	breast:
6	chr6:31364576..31367331-chr6:31369349..31372299,2	MCF-7	breast:
7	chr6:31351876..31353807-chr6:31355261..31357323,2	K562	blood:
8	chr6:31163696..31166940-chr6:31333321..31336541,7	MCF-7	breast:
9	chr6:31343886..31345657-chr6:31346957..31349841,2	MCF-7	breast:
10	chr6:31349465..31351329-chr6:31352381..31354808,2	MCF-7	breast:
11	chr6:31361896..31363850-chr6:31367811..31369632,2	K562	blood:
12	chr6:31163273..31165800-chr6:31352043..31353767,2	K562	blood:
13	chr6:31359042..31360861-chr6:31365962..31368403,2	K562	blood:
14	chr6:31365716..31368807-chr6:31460300..31464467,6	K562	blood:
15	chr6:31353315..31356126-chr6:31366326..31369163,2	K562	blood:
16	chr6:31364571..31365539-chr6:31409150..31410099,3	K562	blood:
17	chr6:31353203..31355935-chr6:31360081..31361637,2	K562	blood:
18	chr6:31358677..31361549-chr6:31370726..31372797,2	MCF-7	breast:
19	chr6:31164859..31165402-chr6:31336129..31336993,3	MCF-7	breast:
20	chr6:31122395..31124246-chr6:31365438..31367824,2	K562	blood:
21	chr6:31360505..31362083-chr6:31379548..31382178,2	K562	blood:
22	chr6:31351876..31353807-chr6:31355261..31357323,2	K562	blood:
23	chr6:31365633..31368446-chr6:31455455..31458235,2	K562	blood:
24	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
25	chr6:31346282..31347893-chr6:31349953..31352420,2	K562	blood:
26	chr6:31363916..31365693-chr6:31369215..31371769,3	K562	blood:
27	chr6:31364413..31365395-chr6:31409114..31409825,5	MCF-7	breast:
28	chr6:31353203..31355935-chr6:31360081..31361637,2	K562	blood:
29	chr6:31122395..31124260-chr6:31365438..31367506,2	K562	blood:
30	chr6:31164797..31165692-chr6:31334361..31335283,4	K562	blood:
31	chr6:31365846..31369030-chr6:31460300..31464467,7	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-B-2	chr6:31362066-31363272	ENSG00000272221.1
2	lnc-MICA-6	chr6:31350312-31351479	NONHSAT108763
3	lnc-HLA-B-2	chr6:31362184-31362994	NONHSAT108766
4	lnc-HLA-B-2	chr6:31362579-31362994	NONHSAT108767
5	lnc-MICA-5	chr6:31360224-31360751	NONHSAT108765
6	lnc-HLA-B-1	chr6:31352905-31352944	NONHSAT108764
7	lnc-HLA-B-2	chr6:31365836-31366051	NONHSAT108766
8	lnc-HLA-B-1	chr6:31350626-31350967	NONHSAT108764
9	lnc-MICA-7	chr6:31348188-31348616	NONHSAT108761

No data

Variant related genes	Relation type
FGFR3P1	TF binding region
RNU6-283P	TF binding region
HLA-S	TF binding region
ZDHHC20P2	TF binding region
ENSG00000265294	TF binding region
DHFRP2	TF binding region
HCP5	TF binding region
ENSG00000272221	TF binding region
HLA-B	TF binding region
FGFR3P1	CpG island
RNU6-283P	CpG island
HLA-S	CpG island
ZDHHC20P2	CpG island
ENSG00000265294	CpG island
DHFRP2	CpG island
HCP5	CpG island
ENSG00000272221	CpG island
HLA-B	CpG island
ENSG00000225851	chromatin interactions
ENSG00000204516	chromatin interactions
ENSG00000230174	chromatin interactions
ENSG00000223702	chromatin interactions
ENSG00000199332	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000272501	chromatin interactions
ENSG00000204520	chromatin interactions
ENSG00000230994	chromatin interactions
ENSG00000206337	chromatin interactions
ENSG00000204536	chromatin interactions
ENSG00000204540	chromatin interactions

Extended variants
information (count: 2002 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:2002 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2523575	chr6:31328826-31328827	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62396277	chr6:31328831-31328832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs55732066	chr6:31328833-31328834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558676440	chr6:31328845-31328846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs180888121	chr6:31328853-31328854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2523574	chr6:31328855-31328856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs548116600	chr6:31328856-31328857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115860766	chr6:31328860-31328861	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
9	rs7772305	chr6:31328886-31328887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552401641	chr6:31328889-31328890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570867288	chr6:31328907-31328908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142459005	chr6:31328923-31328924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553526375	chr6:31328928-31328929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115457991	chr6:31328944-31328945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535939081	chr6:31328950-31328951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116280898	chr6:31328957-31328958	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs116382538	chr6:31328972-31328973	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs115497794	chr6:31328974-31328975	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs2523573	chr6:31328988-31328989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs115955570	chr6:31329001-31329002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114708313	chr6:31329004-31329005	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
22	rs151315805	chr6:31329011-31329012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141977764	chr6:31329023-31329024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114029601	chr6:31329029-31329030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145736797	chr6:31329053-31329054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs118088983	chr6:31329073-31329074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570732592	chr6:31329077-31329078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs202151830	chr6:31329083-31329084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537484383	chr6:31329086-31329087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368552951	chr6:31329087-31329088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547052909	chr6:31329092-31329093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201274214	chr6:31329093-31329094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112515516	chr6:31329100-31329101	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
34	rs551009512	chr6:31329110-31329111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62396278	chr6:31329119-31329120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs2428493	chr6:31329135-31329136	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs147765480	chr6:31329158-31329159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573233101	chr6:31329172-31329173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185889812	chr6:31329179-31329180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34955377	chr6:31329197-31329198	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs192031056	chr6:31329212-31329213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557425857	chr6:31329230-31329231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377480052	chr6:31329231-31329232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370211621	chr6:31329236-31329237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34277309	chr6:31329245-31329246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150321061	chr6:31329249-31329250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575370747	chr6:31329260-31329261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546007982	chr6:31329266-31329267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564258115	chr6:31329274-31329275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2596544	chr6:31329291-31329292	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:125)

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	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
Ovarian cancer	21781307	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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	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
Myelofibrosis	22110671	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
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31325400-31334600	Weak transcription	Pancreas	Pancrea
2	chr6:31327200-31331000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr6:31327200-31331400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr6:31328200-31331000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:31328400-31332000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr6:31330600-31330800	ZNF genes & repeats	Lung	lung
7	chr6:31330800-31333200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr6:31330800-31334600	Weak transcription	Lung	lung
9	chr6:31331000-31331200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr6:31331000-31333400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr6:31331200-31331600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr6:31331400-31331600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr6:31331400-31332400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr6:31331600-31332000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:31331600-31332600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:31332000-31332200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr6:31332000-31332200	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr6:31332400-31334200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:31332600-31334200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:31333200-31333800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
21	chr6:31333800-31334200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr6:31334000-31334400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
23	chr6:31334200-31334400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr6:31334200-31334400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
25	chr6:31334200-31334400	Enhancers	Primary B cells from peripheral blood	blood
26	chr6:31334200-31334400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr6:31334200-31334400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr6:31334200-31334400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr6:31334200-31334400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr6:31334200-31334400	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr6:31334200-31334400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr6:31334200-31334400	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr6:31334200-31334400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr6:31334200-31334400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
35	chr6:31334200-31334400	Enhancers	GM12878-XiMat	blood
36	chr6:31334200-31335000	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr6:31334400-31334600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
38	chr6:31334400-31334600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:31334400-31334600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
40	chr6:31334400-31334600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
41	chr6:31334400-31334600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
42	chr6:31334400-31334600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr6:31334400-31334600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr6:31334400-31334600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr6:31334400-31334600	Active TSS	Brain Angular Gyrus	brain
46	chr6:31334400-31334600	Flanking Active TSS	Brain Cingulate Gyrus	brain
47	chr6:31334400-31334600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
48	chr6:31334400-31334600	Enhancers	Brain Substantia Nigra	brain
49	chr6:31334400-31334600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
50	chr6:31334400-31334600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum

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