Variant report

Variant	esv3360095
Chromosome Location	chr6:31944273-32014622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:994)
CpG islands
(count:4946)
Chromatin interactive
region (count:19)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	ARID3A	chr6:32014416-32014548	K562	blood:	n/a	n/a
3	ATF1	chr6:32013622-32013705	K562	blood:	n/a	n/a
4	ATF3	chr6:32014165-32014416	K562	blood:	n/a	n/a
5	BHLHE40	chr6:32013765-32014659	K562	blood:	n/a	n/a
6	BHLHE40	chr6:31982297-31982618	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:32007706-32008062	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:31970701-31971047	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:31947116-31947502	K562	blood:	n/a	n/a
10	BHLHE40	chr6:32012916-32012940	K562	blood:	n/a	n/a
11	BHLHE40	chr6:32003438-32003784	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:31949559-31949880	HepG2	liver:	n/a	n/a
13	CBX3	chr6:31990799-31991208	K562	blood:	n/a	n/a
14	CBX3	chr6:31946996-31947474	K562	blood:	n/a	n/a
15	CBX3	chr6:31957963-31958493	K562	blood:	n/a	n/a
16	CBX3	chr6:31989858-31990273	K562	blood:	n/a	n/a
17	CBX3	chr6:31985480-31985931	K562	blood:	n/a	n/a
18	CBX3	chr6:31970387-31971162	K562	blood:	n/a	n/a
19	CBX3	chr6:32003387-32003757	K562	blood:	n/a	n/a
20	CBX3	chr6:31980155-31981063	K562	blood:	n/a	n/a
21	CBX3	chr6:31952664-31953239	K562	blood:	n/a	n/a
22	CBX3	chr6:31952793-31953135	K562	blood:	n/a	n/a
23	CBX3	chr6:31985535-31985921	K562	blood:	n/a	n/a
24	CBX3	chr6:32003260-32004138	K562	blood:	n/a	n/a
25	CBX3	chr6:31990712-31991199	K562	blood:	n/a	n/a
26	CBX3	chr6:31958022-31958441	K562	blood:	n/a	n/a
27	CBX3	chr6:31982302-31982628	K562	blood:	n/a	n/a
28	CBX3	chr6:31970603-31971015	K562	blood:	n/a	n/a
29	CBX3	chr6:32012704-32014465	K562	blood:	n/a	n/a
30	CBX3	chr6:31965417-31965721	K562	blood:	n/a	n/a
31	CBX3	chr6:31989920-31990157	K562	blood:	n/a	n/a
32	CCNT2	chr6:31947256-31947610	K562	blood:	n/a	n/a
33	CEBPB	chr6:32003276-32004129	K562	blood:	n/a	n/a
34	CEBPB	chr6:31970725-31971176	K562	blood:	n/a	n/a
35	CEBPB	chr6:32014177-32015205	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr6:32003420-32003920	K562	blood:	n/a	n/a
37	CEBPB	chr6:31970574-31971273	K562	blood:	n/a	n/a
38	CEBPD	chr6:31980664-31980987	K562	blood:	n/a	n/a
39	CEBPD	chr6:32013475-32013869	K562	blood:	n/a	n/a
40	CEBPD	chr6:31972233-31972447	HepG2	liver:	n/a	n/a
41	CEBPD	chr6:31970600-31971236	K562	blood:	n/a	n/a
42	CEBPD	chr6:32003343-32003982	K562	blood:	n/a	n/a
43	CHD2	chr6:32014592-32015350	HepG2	liver:	n/a	n/a
44	CHD2	chr6:32014215-32014435	K562	blood:	n/a	n/a
45	CHD2	chr6:31947206-31947389	K562	blood:	n/a	n/a
46	CHD2	chr6:32014382-32015277	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr6:31957626-31957645	K562	blood:	n/a	n/a
48	CTCF	chr6:32008734-32008854	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr6:31957289-31957387	HepG2	liver:	n/a	n/a
50	CTCF	chr6:31957304-31957419	GM13976	blood:	n/a	n/a

(count:4946 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32014189-32014239	Hela-S3	cervix:	n/a
2	chr6:32012897-32012947	BE2_C	brain:	n/a
3	chr6:31980043-31980093	HRPEpiC	eye:	n/a
4	chr6:31997491-31997541	HMEC	breast:	n/a
5	chr6:32014300-32014350	BJ	skin:	n/a
6	chr6:32014189-32014239	Hela-S3	cervix:	n/a
7	chr6:32012897-32012947	BE2_C	brain:	n/a
8	chr6:31980043-31980093	HRPEpiC	eye:	n/a
9	chr6:31997491-31997541	HMEC	breast:	n/a
10	chr6:32014300-32014350	BJ	skin:	n/a
11	chr6:32007986-32008036	U87	brain:	n/a
12	chr6:31973162-31973212	ovcar-3	ovarian:	n/a
13	chr6:31980043-31980093	HNPCEpiC	eye:	n/a
14	chr6:31964193-31964243	SAEC	small airway:	n/a
15	chr6:31963912-31963962	GM12878	blood:	n/a
16	chr6:31973180-31973230	LNCaP	prostate:	n/a
17	chr6:32012897-32012947	NHDF-neo	bronchial:	n/a
18	chr6:32014059-32014109	LNCaP	prostate:	n/a
19	chr6:31973345-31973395	SKMC	muscle:	n/a
20	chr6:32014510-32014560	PrEC	prostate:	n/a
21	chr6:31948433-31948483	PANC-1	pancreas:	n/a
22	chr6:31963892-31963942	Hela-S3	cervix:	n/a
23	chr6:32011583-32011633	GM12892	blood:	n/a
24	chr6:31948433-31948483	AG04449	skin:	fetal
25	chr6:32005786-32005836	H1-hESC	embryonic stem cell:	embryo
26	chr6:31977599-31977649	IMR90	lung:	fetal
27	chr6:31973162-31973212	NH-A	brain:	n/a
28	chr6:31980043-31980093	HCT-116	colon:	n/a
29	chr6:32007916-32007966	HEK293	kidney:	embryo
30	chr6:32014484-32014534	AG10803	skin:	n/a
31	chr6:32014484-32014534	HUVEC	blood vessel:	n/a
32	chr6:31977599-31977649	HEK293	kidney:	embryo
33	chr6:31964274-31964324	U87	brain:	n/a
34	chr6:32013845-32013895	GM12892	blood:	n/a
35	chr6:31964754-31964804	HCF	heart:	n/a
36	chr6:32014189-32014239	GM12878	blood:	n/a
37	chr6:32011687-32011737	GM12892	blood:	n/a
38	chr6:32009422-32009472	H1-hESC	embryonic stem cell:	embryo
39	chr6:31973255-31973305	AG10803	skin:	n/a
40	chr6:31963912-31963962	MCF-7	breast:	n/a
41	chr6:31977599-31977649	HL-60	blood:	n/a
42	chr6:32011575-32011625	H1-hESC	embryonic stem cell:	embryo
43	chr6:31964288-31964338	MCF-7	breast:	n/a
44	chr6:32010333-32010383	PFSK-1	brain:	n/a
45	chr6:32014059-32014109	AG04449	skin:	fetal
46	chr6:31977506-31977556	PANC-1	pancreas:	n/a
47	chr6:31973255-31973305	NH-A	brain:	n/a
48	chr6:31963892-31963942	SK-N-MC	brain:	n/a
49	chr6:31947216-31947266	HRPEpiC	eye:	n/a
50	chr6:31977506-31977556	NHBE	bronchial:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31928405..31931072-chr6:32014405..32017248,2	K562	blood:
2	chr6:31938465..31941001-chr6:32013795..32015947,2	K562	blood:
3	chr6:31939757..31942101-chr6:31945170..31946681,2	MCF-7	breast:
4	chr6:31631447..31633355-chr6:32013677..32016476,2	K562	blood:
5	chr6:31938987..31942159-chr6:31944563..31949146,6	MCF-7	breast:
6	chr6:31868360..31871056-chr6:32011358..32014091,3	K562	blood:
7	chr6:31830912..31833686-chr6:32013315..32015593,2	K562	blood:
8	chr6:32014542..32017547-chr6:32094329..32097985,3	MCF-7	breast:
9	chr6:31912743..31916758-chr6:31944927..31949257,3	K562	blood:
10	chr6:32013434..32015953-chr6:32095466..32097702,3	K562	blood:
11	chr6:31830409..31832412-chr6:32014093..32016041,2	K562	blood:
12	chr6:31942872..31944995-chr6:31945602..31947242,2	MCF-7	breast:
13	chr6:31935647..31937211-chr6:31946410..31948036,2	K562	blood:
14	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:
15	chr6:31868623..31870778-chr6:31945874..31948322,2	K562	blood:
16	chr6:31868360..31870239-chr6:32012136..32014091,2	K562	blood:
17	chr6:31942872..31944995-chr6:31945602..31947242,2	MCF-7	breast:
18	chr6:31938465..31944613-chr6:32012205..32018958,7	K562	blood:
19	chr6:31938465..31944613-chr6:32012205..32018958,7	K562	blood:

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

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

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
CYP21A1P	TF binding region
C4B	TF binding region
C4B-AS1	TF binding region
DXO	TF binding region
CYP21A2	TF binding region
STK19	TF binding region
ENSG00000268923	TF binding region
TNXB	TF binding region
C4A-AS1	TF binding region
C4A	TF binding region
TNXA	CpG island
STK19P	CpG island
CYP21A1P	CpG island
C4B	CpG island
C4B-AS1	CpG island
DXO	CpG island
CYP21A2	CpG island
STK19	CpG island
ENSG00000268923	CpG island
TNXB	CpG island
C4A-AS1	CpG island
C4A	CpG island
ENSG00000168477	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000204351	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000213676	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000243649	chromatin interactions

Extended variants
information (count: 1273 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536492407	chr6:31944273-31944274	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs376394457	chr6:31944279-31944280	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs547921	chr6:31944320-31944321	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs566984017	chr6:31944321-31944322	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs2854435	chr6:31944375-31944376	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555861420	chr6:31944414-31944415	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs577596295	chr6:31944421-31944422	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs544958709	chr6:31944425-31944426	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs540169771	chr6:31944426-31944427	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs572268107	chr6:31944433-31944434	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs561627815	chr6:31944506-31944507	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs542802501	chr6:31944561-31944562	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs528880481	chr6:31944568-31944569	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs550671	chr6:31944593-31944594	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576577977	chr6:31944594-31944595	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs543922819	chr6:31944605-31944606	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs565116870	chr6:31944645-31944646	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs368981883	chr6:31944648-31944649	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs532576056	chr6:31944655-31944656	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs547767962	chr6:31944666-31944667	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs559570536	chr6:31944679-31944680	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs530339126	chr6:31944689-31944690	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs372501699	chr6:31944704-31944705	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs569940671	chr6:31944729-31944730	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs375784544	chr6:31944733-31944734	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs549883370	chr6:31944745-31944746	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs369783273	chr6:31944775-31944776	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs574756851	chr6:31944785-31944786	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs6905149	chr6:31944790-31944791	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs553807424	chr6:31944797-31944798	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs572336087	chr6:31944845-31944846	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs41315816	chr6:31944851-31944852	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs114492815	chr6:31944884-31944885	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs576219527	chr6:31944895-31944896	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs56069943	chr6:31944910-31944911	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs56005017	chr6:31944954-31944955	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs138596753	chr6:31944956-31944957	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs376215500	chr6:31944962-31944963	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs193114370	chr6:31944967-31944968	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs9404990	chr6:31945056-31945057	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs577268025	chr6:31945090-31945091	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs551133920	chr6:31945116-31945117	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs113373502	chr6:31945143-31945144	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs541378168	chr6:31945150-31945151	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs374551817	chr6:31945151-31945152	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs12524149	chr6:31945230-31945231	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs575678434	chr6:31945256-31945257	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs11961695	chr6:31945267-31945268	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs554400129	chr6:31945288-31945289	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs548501910	chr6:31945289-31945290	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	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:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31941000-31946600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:31941000-31946600	Weak transcription	Left Ventricle	heart
3	chr6:31941000-31946600	Weak transcription	Lung	lung
4	chr6:31941000-31947200	Weak transcription	Esophagus	oesophagus
5	chr6:31941000-31947200	Weak transcription	Ovary	ovary
6	chr6:31941000-31947200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr6:31941000-31947600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:31941000-31949600	Weak transcription	Right Ventricle	heart
9	chr6:31941000-31949800	Weak transcription	Gastric	stomach
10	chr6:31941200-31944400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr6:31941200-31945400	Weak transcription	Fetal Muscle Leg	muscle
12	chr6:31941200-31945800	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr6:31941200-31946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:31941200-31946400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr6:31941200-31946400	Weak transcription	Placenta	Placenta
16	chr6:31941200-31946400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr6:31941200-31946600	Weak transcription	Primary B cells from peripheral blood	blood
18	chr6:31941200-31946600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr6:31941200-31947000	Weak transcription	Pancreas	Pancrea
20	chr6:31941200-31947200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr6:31941200-31947200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr6:31941200-31947200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr6:31941200-31947200	Weak transcription	Spleen	Spleen
24	chr6:31941200-31947400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:31941200-31949200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr6:31941200-31949400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr6:31941200-31949400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr6:31941200-31950000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr6:31941400-31944600	Weak transcription	Brain Germinal Matrix	brain
30	chr6:31941400-31944800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:31941400-31945800	Weak transcription	Primary T cells from cord blood	blood
32	chr6:31941400-31945800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr6:31941400-31945800	Weak transcription	Fetal Brain Female	brain
34	chr6:31941400-31946000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr6:31941400-31946600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr6:31941400-31946600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:31941400-31946600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr6:31941400-31946600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr6:31941400-31946600	Weak transcription	Thymus	Thymus
40	chr6:31941400-31947000	Weak transcription	Adipose Nuclei	Adipose
41	chr6:31941400-31947200	Weak transcription	Brain Anterior Caudate	brain
42	chr6:31941400-31947200	Weak transcription	Brain Substantia Nigra	brain
43	chr6:31941400-31947200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr6:31941400-31947200	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr6:31941400-31947400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr6:31941400-31947600	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr6:31941400-31949000	Weak transcription	Colonic Mucosa	Colon
48	chr6:31941400-31949400	Weak transcription	Primary B cells from cord blood	blood
49	chr6:31941400-31949400	Weak transcription	NH-A	brain
50	chr6:31941400-31950000	Weak transcription	Fetal Kidney	kidney

The 2.0 version of rSNPBase

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