Variant report

Variant	esv988873
Chromosome Location	chr6:34548881-34557080
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr6:34551355-34551428	K562	blood:	n/a	n/a
2	CEBPB	chr6:34553230-34553567	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr6:34553182-34553630	IMR90	lung:	n/a	n/a
4	CEBPB	chr6:34553231-34553535	A549	lung:	n/a	n/a
5	CEBPB	chr6:34553219-34553507	K562	blood:	n/a	n/a
6	CTCF	chr6:34551198-34551486	NHEK	skin:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
7	CTCF	chr6:34551260-34551410	AoAF	blood vessel:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
8	CTCF	chr6:34551280-34551430	HPF	lung:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
9	CTCF	chr6:34551280-34551430	NHEK	skin:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
10	CTCF	chr6:34551303-34551381	MCF-7	breast:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
11	CTCF	chr6:34551220-34551370	HEK293	kidney:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
12	CTCF	chr6:34552500-34552650	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr6:34551149-34551505	K562	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
14	CTCF	chr6:34551240-34551390	SK-N-SH_RA	brain:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
15	CTCF	chr6:34551240-34551390	HFF	foreskin:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
16	CTCF	chr6:34551260-34551410	GM12869	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
17	CTCF	chr6:34551260-34551410	BJ	skin:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
18	CTCF	chr6:34551420-34551570	GM12867	blood:	n/a	n/a
19	CTCF	chr6:34551360-34551510	HVMF	connective:	n/a	n/a
20	CTCF	chr6:34551300-34551450	AG04449	skin:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
21	CTCF	chr6:34551316-34551321	GM12891	blood:	n/a	n/a
22	CTCF	chr6:34551380-34551530	GM12875	blood:	n/a	n/a
23	CTCF	chr6:34551380-34551530	HAc	cerebellar:	n/a	n/a
24	CTCF	chr6:34551320-34551470	AG10803	skin:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
25	CTCF	chr6:34551231-34551450	GM19239	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
26	CTCF	chr6:34551300-34551413	GM10266	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
27	CTCF	chr6:34551000-34551558	A549	lung:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
28	CTCF	chr6:34551260-34551410	AG04450	lung:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
29	CTCF	chr6:34551182-34551431	A549	lung:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
30	CTCF	chr6:34551260-34551410	BE2_C	brain:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
31	CTCF	chr6:34551280-34551430	GM12865	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
32	CTCF	chr6:34551220-34551370	HCM	heart:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
33	CTCF	chr6:34551311-34551375	MCF-7	breast:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
34	CTCF	chr6:34551260-34551410	HPF	lung:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
35	CTCF	chr6:34550990-34551541	SK-N-SH	brain:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
36	CTCF	chr6:34551300-34551450	HCPEpiC	choroid plexus:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
37	CTCF	chr6:34551280-34551430	GM06990	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
38	CTCF	chr6:34551260-34551410	WERI-Rb-1	eye:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
39	CTCF	chr6:34551280-34551430	HBMEC	blood vessel:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
40	CTCF	chr6:34551300-34551450	HCFaa	heart:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
41	CTCF	chr6:34551980-34552130	HEK293	kidney:	n/a	n/a
42	CTCF	chr6:34551260-34551410	SK-N-SH_RA	brain:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
43	CTCF	chr6:34551240-34551390	AG09319	gingival:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
44	CTCF	chr6:34552500-34552650	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr6:34551180-34551330	GM12874	blood:	n/a	n/a
46	CTCF	chr6:34553280-34553430	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr6:34551293-34551403	Spleen_OC	spleen:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
48	CTCF	chr6:34551260-34551410	GM12870	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345
49	CTCF	chr6:34553300-34553450	AG10803	skin:	n/a	n/a
50	CTCF	chr6:34551310-34551410	GM13976	blood:	n/a	chr6:34551329-34551347 chr6:34551324-34551345

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34554635-34554685	HEK293	kidney:	embryo
2	chr6:34554635-34554685	HEK293	kidney:	embryo
3	chr6:34554635-34554685	AG09309	skin:	n/a
4	chr6:34554635-34554685	PrEC	prostate:	n/a
5	chr6:34554635-34554685	NB4	blood:	n/a
6	chr6:34554635-34554685	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:34556105-34556155	HL-60	blood:	n/a
8	chr6:34556105-34556155	Hepatocyte	liver:	n/a
9	chr6:34556105-34556155	AG04449	skin:	fetal
10	chr6:34556105-34556155	CMK	blood:	n/a
11	chr6:34556105-34556155	Caco-2	colon:	n/a
12	chr6:34556105-34556155	T-47D	breast:	n/a
13	chr6:34554635-34554685	HCM	heart:	n/a
14	chr6:34556105-34556155	H1-hESC	embryonic stem cell:	embryo
15	chr6:34554635-34554685	BE2_C	brain:	n/a
16	chr6:34556105-34556155	NB4	blood:	n/a
17	chr6:34556105-34556155	HRE	kidney:	n/a
18	chr6:34556105-34556155	AG04450	lung:	fetal
19	chr6:34556105-34556155	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:34554635-34554685	GM06990	blood:	n/a
21	chr6:34554635-34554685	SAEC	small airway:	n/a
22	chr6:34554635-34554685	GM12878	blood:	n/a
23	chr6:34556105-34556155	IMR90	lung:	fetal
24	chr6:34556105-34556155	ProgFib	skin:	n/a
25	chr6:34554635-34554685	T-47D	breast:	n/a
26	chr6:34554635-34554685	BJ	skin:	n/a
27	chr6:34554635-34554685	AG10803	skin:	n/a
28	chr6:34554635-34554685	HRPEpiC	eye:	n/a
29	chr6:34556105-34556155	A549	lung:	n/a
30	chr6:34554635-34554685	A549	lung:	n/a
31	chr6:34556105-34556155	GM12878	blood:	n/a
32	chr6:34556105-34556155	HRPEpiC	eye:	n/a
33	chr6:34554635-34554685	AG09319	gingival:	n/a
34	chr6:34556105-34556155	NH-A	brain:	n/a
35	chr6:34556105-34556155	HCF	heart:	n/a
36	chr6:34554635-34554685	Caco-2	colon:	n/a
37	chr6:34556105-34556155	AG09309	skin:	n/a
38	chr6:34554635-34554685	MCF-7	breast:	n/a
39	chr6:34554635-34554685	NHBE	bronchial:	n/a
40	chr6:34554635-34554685	CMK	blood:	n/a
41	chr6:34554635-34554685	HUVEC	blood vessel:	n/a
42	chr6:34556105-34556155	U87	brain:	n/a
43	chr6:34554635-34554685	K562	blood:	n/a
44	chr6:34556105-34556155	SK-N-SH_RA	brain:	n/a
45	chr6:34556105-34556155	SK-N-SH	brain:	n/a
46	chr6:34556105-34556155	MCF-7	breast:	n/a
47	chr6:34554635-34554685	U87	brain:	n/a
48	chr6:34556105-34556155	AoSMC	blood vessel:	n/a
49	chr6:34554635-34554685	SKMC	muscle:	n/a
50	chr6:34554635-34554685	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:34535538..34537048-chr6:34550660..34552218,2	K562	blood:
2	chr6:34552512..34555793-chr6:34557456..34559676,4	K562	blood:
3	chr6:34555563..34557937-chr6:34565420..34567500,2	MCF-7	breast:
4	chr6:34556477..34558715-chr6:34566152..34568082,2	K562	blood:
5	chr6:34543118..34546056-chr6:34551704..34553815,2	K562	blood:
6	chr6:34543493..34547191-chr6:34549783..34553774,3	MCF-7	breast:
7	chr6:34546025..34550946-chr6:34551862..34556143,7	K562	blood:
8	chr6:34546025..34550946-chr6:34551862..34556143,7	K562	blood:
9	chr6:34172530..34175474-chr6:34548744..34550732,2	K562	blood:
10	chr6:34553634..34556369-chr6:34563010..34564695,2	MCF-7	breast:
11	chr6:34552512..34555793-chr6:34557456..34559676,3	K562	blood:
12	chr6:34544085..34546568-chr6:34548676..34550221,2	K562	blood:
13	chr6:34551284..34553223-chr6:34555958..34557670,2	MCF-7	breast:
14	chr6:34550788..34556388-chr6:34565460..34570894,5	K562	blood:
15	chr6:34553065..34556672-chr6:34559907..34563488,3	K562	blood:
16	chr6:34543365..34546387-chr6:34554474..34557693,3	K562	blood:
17	chr6:34522438..34524089-chr6:34549801..34552822,3	MCF-7	breast:
18	chr6:34548787..34550337-chr6:34551862..34554295,2	K562	blood:
19	chr6:34548787..34550337-chr6:34551862..34554295,2	K562	blood:
20	chr6:34493240..34495795-chr6:34548549..34550240,2	K562	blood:
21	chr6:34544544..34547164-chr6:34547916..34551672,4	K562	blood:
22	chr6:34551284..34553223-chr6:34555958..34557670,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196114	TF binding region
ENSG00000196114	CpG island
ENSG00000196114	chromatin interactions

Extended variants
information (count: 327 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538556164	chr6:34548921-34548922	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs550089396	chr6:34548950-34548951	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs372876559	chr6:34548951-34548952	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs149646184	chr6:34548957-34548958	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs58028667	chr6:34548992-34548993	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs377332471	chr6:34549043-34549044	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs62398730	chr6:34549064-34549065	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs143377900	chr6:34549100-34549101	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs451603	chr6:34549107-34549108	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs527265971	chr6:34549110-34549111	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs74550710	chr6:34549156-34549157	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148353937	chr6:34549161-34549162	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567996323	chr6:34549197-34549198	Enhancers Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs74672435	chr6:34549258-34549259	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141497692	chr6:34549289-34549290	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs576969242	chr6:34549295-34549296	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527257686	chr6:34549307-34549308	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545131141	chr6:34549364-34549365	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560584238	chr6:34549369-34549370	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527656020	chr6:34549489-34549490	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs451263	chr6:34549498-34549499	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs372826534	chr6:34549499-34549500	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147509926	chr6:34549511-34549512	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs367718916	chr6:34549528-34549529	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531903652	chr6:34549570-34549571	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550499267	chr6:34549592-34549593	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187132743	chr6:34549676-34549677	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76883302	chr6:34549683-34549684	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs412392	chr6:34549699-34549700	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs547054832	chr6:34549739-34549740	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565461103	chr6:34549745-34549746	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs189919535	chr6:34549755-34549756	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554129097	chr6:34549766-34549767	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140435003	chr6:34549776-34549777	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569679884	chr6:34549778-34549779	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374133388	chr6:34549780-34549781	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536899728	chr6:34549783-34549784	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558823680	chr6:34549803-34549804	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs1201874	chr6:34549810-34549811	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs541245780	chr6:34549817-34549818	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181966456	chr6:34549903-34549904	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572554269	chr6:34549922-34549923	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs114193881	chr6:34549926-34549927	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs186136610	chr6:34549954-34549955	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs142738537	chr6:34549984-34549985	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs56350128	chr6:34549997-34549998	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189767472	chr6:34549998-34549999	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565590284	chr6:34550009-34550010	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs73409969	chr6:34550012-34550013	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs547564083	chr6:34550013-34550014	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	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
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
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
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
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34528800-34551400	Weak transcription	Right Atrium	heart
2	chr6:34535600-34563200	Weak transcription	A549	lung
3	chr6:34536800-34554400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:34536800-34556600	Weak transcription	Hela-S3	cervix
5	chr6:34537400-34552800	Weak transcription	Fetal Intestine Large	intestine
6	chr6:34538000-34555400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr6:34538800-34550600	Weak transcription	Esophagus	oesophagus
8	chr6:34538800-34552600	Weak transcription	Right Ventricle	heart
9	chr6:34539600-34552800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:34540800-34554000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:34541600-34553200	Weak transcription	Lung	lung
12	chr6:34541800-34553400	Weak transcription	HepG2	liver
13	chr6:34542000-34553000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:34542200-34555400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:34542400-34553800	Weak transcription	Liver	Liver
16	chr6:34543200-34549000	Weak transcription	Fetal Intestine Small	intestine
17	chr6:34543200-34552200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:34544200-34555000	Weak transcription	Pancreas	Pancrea
19	chr6:34544400-34551200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:34544600-34549000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr6:34544600-34553600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:34544600-34553800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:34544800-34549000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr6:34544800-34551000	Weak transcription	Placenta	Placenta
25	chr6:34545000-34550800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr6:34545000-34554400	Weak transcription	NHEK	skin
27	chr6:34545200-34552600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:34545200-34552800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:34545400-34549000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr6:34545400-34554000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr6:34545600-34550000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:34545800-34551400	Weak transcription	Primary T cells from cord blood	blood
33	chr6:34545800-34552600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:34545800-34553200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr6:34546000-34554000	Weak transcription	Fetal Thymus	thymus
36	chr6:34546000-34559800	Weak transcription	HSMM	muscle
37	chr6:34546200-34553000	Weak transcription	K562	blood
38	chr6:34546400-34555600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr6:34546600-34552600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr6:34546600-34552600	Weak transcription	Gastric	stomach
41	chr6:34546600-34553000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr6:34546600-34553200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:34546800-34552400	Weak transcription	Adipose Nuclei	Adipose
44	chr6:34547200-34553200	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr6:34547200-34555600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr6:34547200-34566800	Weak transcription	Aorta	Aorta
47	chr6:34547400-34553400	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr6:34547600-34550400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:34547600-34555400	Weak transcription	Primary B cells from cord blood	blood
50	chr6:34547800-34549400	Enhancers	Brain Germinal Matrix	brain

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