Variant report

Variant	nsv886767
Chromosome Location	chr6:150335407-150400488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1506)
CpG islands
(count:2932)
Chromatin interactive
region (count:44)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1506 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150399954-150400171	K562	blood:	n/a	n/a
2	ARID3A	chr6:150338070-150338270	HepG2	liver:	n/a	n/a
3	ATF1	chr6:150336933-150337019	K562	blood:	n/a	n/a
4	ATF1	chr6:150399918-150400184	K562	blood:	n/a	n/a
5	ATF3	chr6:150393282-150393683	K562	blood:	n/a	n/a
6	ATF3	chr6:150393387-150393675	K562	blood:	n/a	n/a
7	BACH1	chr6:150390043-150390558	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:150346621-150346888	GM12878	blood:	n/a	chr6:150346723-150346734 chr6:150346728-150346738 chr6:150346724-150346734
9	BHLHE40	chr6:150381363-150381384	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:150336771-150337140	K562	blood:	n/a	n/a
11	BHLHE40	chr6:150381236-150381439	K562	blood:	n/a	n/a
12	BHLHE40	chr6:150381181-150381607	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:150393464-150393645	K562	blood:	n/a	n/a
14	BHLHE40	chr6:150400020-150400054	K562	blood:	n/a	n/a
15	BRCA1	chr6:150393387-150393635	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr6:150390134-150390251	HepG2	liver:	n/a	n/a
17	BRCA1	chr6:150389971-150390353	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr6:150389949-150390617	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr6:150390049-150390278	GM12878	blood:	n/a	n/a
20	CBX3	chr6:150392124-150392644	K562	blood:	n/a	n/a
21	CBX3	chr6:150336795-150337204	K562	blood:	n/a	n/a
22	CBX3	chr6:150388339-150388656	K562	blood:	n/a	n/a
23	CBX3	chr6:150393286-150393679	K562	blood:	n/a	n/a
24	CCNT2	chr6:150393445-150393693	K562	blood:	n/a	n/a
25	CCNT2	chr6:150399968-150400225	K562	blood:	n/a	n/a
26	CCNT2	chr6:150390227-150390513	K562	blood:	n/a	n/a
27	CCNT2	chr6:150336957-150337116	K562	blood:	n/a	n/a
28	CEBPB	chr6:150393339-150393679	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr6:150349144-150349326	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:150338134-150338334	K562	blood:	n/a	n/a
31	CEBPB	chr6:150338074-150338240	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:150399928-150400215	K562	blood:	n/a	n/a
33	CEBPB	chr6:150338040-150338336	A549	lung:	n/a	n/a
34	CEBPB	chr6:150338050-150338338	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:150338040-150338363	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr6:150339700-150339896	HepG2	liver:	n/a	chr6:150339786-150339797
37	CEBPB	chr6:150389394-150389606	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr6:150339733-150339933	Hela-S3	cervix:	n/a	chr6:150339786-150339797
39	CEBPB	chr6:150353985-150354064	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:150394975-150395180	HepG2	liver:	n/a	chr6:150395108-150395119
41	CEBPB	chr6:150336946-150337113	K562	blood:	n/a	n/a
42	CEBPB	chr6:150389818-150389873	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr6:150394988-150395223	K562	blood:	n/a	chr6:150395108-150395119
44	CEBPB	chr6:150346556-150346899	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr6:150390170-150390428	Hela-S3	cervix:	n/a	n/a
46	CEBPD	chr6:150399799-150400364	K562	blood:	n/a	n/a
47	CHD2	chr6:150389992-150390390	GM12878	blood:	n/a	n/a
48	CHD2	chr6:150389968-150390504	HepG2	liver:	n/a	n/a
49	CHD2	chr6:150392325-150392525	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr6:150389994-150390364	K562	blood:	n/a	n/a

(count:2932 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150336524-150336574	U87	brain:	n/a
2	chr6:150379047-150379097	HCM	heart:	n/a
3	chr6:150359383-150359433	NHDF-neo	bronchial:	n/a
4	chr6:150379008-150379058	HCF	heart:	n/a
5	chr6:150336524-150336574	U87	brain:	n/a
6	chr6:150379047-150379097	HCM	heart:	n/a
7	chr6:150359383-150359433	NHDF-neo	bronchial:	n/a
8	chr6:150379008-150379058	HCF	heart:	n/a
9	chr6:150376218-150376268	HUVEC	blood vessel:	n/a
10	chr6:150356698-150356748	PANC-1	pancreas:	n/a
11	chr6:150390894-150390944	ECC-1	luminal epithelium:	n/a
12	chr6:150346721-150346771	GM06990	blood:	n/a
13	chr6:150390253-150390303	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:150378972-150379022	BJ	skin:	n/a
15	chr6:150346886-150346936	GM12891	blood:	n/a
16	chr6:150378972-150379022	NB4	blood:	n/a
17	chr6:150390302-150390352	HEK293	kidney:	embryo
18	chr6:150346787-150346837	BE2_C	brain:	n/a
19	chr6:150378738-150378788	HCF	heart:	n/a
20	chr6:150359383-150359433	AG09309	skin:	n/a
21	chr6:150360829-150360879	SK-N-SH_RA	brain:	n/a
22	chr6:150358873-150358923	GM12892	blood:	n/a
23	chr6:150390302-150390352	IMR90	lung:	fetal
24	chr6:150393535-150393585	IMR90	lung:	fetal
25	chr6:150390894-150390944	HIPEpiC	eye:	n/a
26	chr6:150346921-150346971	NHDF-neo	bronchial:	n/a
27	chr6:150346816-150346866	AG10803	skin:	n/a
28	chr6:150378881-150378931	AoSMC	blood vessel:	n/a
29	chr6:150376218-150376268	PrEC	prostate:	n/a
30	chr6:150347012-150347062	GM06990	blood:	n/a
31	chr6:150346921-150346971	AG04449	skin:	fetal
32	chr6:150346863-150346913	NH-A	brain:	n/a
33	chr6:150381200-150381250	A549	lung:	n/a
34	chr6:150381200-150381250	HCF	heart:	n/a
35	chr6:150346921-150346971	HIPEpiC	eye:	n/a
36	chr6:150388100-150388150	NB4	blood:	n/a
37	chr6:150335417-150335467	HepG2	liver:	n/a
38	chr6:150346800-150346850	IMR90	lung:	fetal
39	chr6:150381200-150381250	U87	brain:	n/a
40	chr6:150390267-150390317	HAEpiC	amniotic membrane:	n/a
41	chr6:150390253-150390303	PrEC	prostate:	n/a
42	chr6:150388100-150388150	SKMC	muscle:	n/a
43	chr6:150360829-150360879	HMEC	breast:	n/a
44	chr6:150390894-150390944	H1-hESC	embryonic stem cell:	embryo
45	chr6:150390267-150390317	GM12878	blood:	n/a
46	chr6:150381200-150381250	SK-N-SH	brain:	n/a
47	chr6:150359130-150359180	CMK	blood:	n/a
48	chr6:150336054-150336104	SK-N-MC	brain:	n/a
49	chr6:150346858-150346908	NH-A	brain:	n/a
50	chr6:150335417-150335467	HEEpiC	esophagus:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150378922..150380433-chr6:150385877..150388167,2	K562	blood:
2	chr6:150399642..150402199-chr6:150464178..150465810,2	MCF-7	breast:
3	chr6:150250328..150250903-chr6:150390622..150391573,2	MCF-7	breast:
4	chr6:150255064..150255979-chr6:150337750..150338789,5	K562	blood:
5	chr6:150384794..150386662-chr6:150388680..150390331,2	MCF-7	breast:
6	chr6:150380000..150382934-chr6:150383185..150385012,2	MCF-7	breast:
7	chr6:150379821..150382555-chr6:150387863..150390602,3	MCF-7	breast:
8	chr6:150354931..150357925-chr6:150386556..150388661,2	K562	blood:
9	chr6:150274811..150275321-chr6:150336040..150336549,2	MCF-7	breast:
10	chr6:150400447..150403376-chr6:150651283..150654200,2	K562	blood:
11	chr6:150378184..150381057-chr6:150388223..150390154,2	MCF-7	breast:
12	chr6:150261749..150263311-chr6:150348518..150350047,2	MCF-7	breast:
13	chr6:150392325..150392932-chr6:150655903..150657072,4	K562	blood:
14	chr6:150154861..150155845-chr6:150337730..150338274,2	K562	blood:
15	chr6:150370900..150376205-chr6:150377396..150379934,4	K562	blood:
16	chr6:150361366..150363759-chr6:150390933..150393439,2	K562	blood:
17	chr6:150345687..150347890-chr6:150385680..150387900,2	MCF-7	breast:
18	chr6:150394796..150396864-chr6:150397633..150400539,2	MCF-7	breast:
19	chr6:150391874..150392906-chr6:150655937..150656926,3	MCF-7	breast:
20	chr6:150323301..150326870-chr6:150337464..150339739,3	MCF-7	breast:
21	chr6:150396050..150398924-chr6:150713312..150715436,2	MCF-7	breast:
22	chr6:150354901..150357527-chr6:150362159..150364156,2	MCF-7	breast:
23	chr6:150370900..150373661-chr6:150377798..150379934,2	K562	blood:
24	chr6:150394796..150396864-chr6:150397633..150400539,2	MCF-7	breast:
25	chr6:150324211..150327033-chr6:150387350..150388851,2	K562	blood:
26	chr6:150355810..150358323-chr6:150360175..150362251,2	K562	blood:
27	chr6:150378922..150380433-chr6:150385877..150388167,2	K562	blood:
28	chr6:150155381..150157771-chr6:150346025..150347800,2	MCF-7	breast:
29	chr6:150283429..150285848-chr6:150336024..150337757,2	MCF-7	breast:
30	chr6:150378184..150381057-chr6:150388223..150390154,2	MCF-7	breast:
31	chr6:150370900..150373661-chr6:150377798..150379934,2	K562	blood:
32	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
33	chr6:150354931..150357925-chr6:150386556..150388661,2	K562	blood:
34	chr6:150384115..150385944-chr6:150388643..150390347,3	MCF-7	breast:
35	chr6:150250322..150251340-chr6:150337738..150338572,3	K562	blood:
36	chr6:150258514..150260378-chr6:150337573..150339969,2	MCF-7	breast:
37	chr6:150386654..150388325-chr6:150388815..150391248,2	MCF-7	breast:
38	chr6:150246157..150249113-chr6:150336737..150339289,2	K562	blood:
39	chr6:150355810..150358323-chr6:150360175..150362251,2	K562	blood:
40	chr6:150350371..150352271-chr6:150387708..150390265,2	MCF-7	breast:
41	chr6:150380000..150382934-chr6:150383185..150385012,2	MCF-7	breast:
42	chr6:150370900..150376205-chr6:150377396..150379934,4	K562	blood:
43	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
44	chr6:150396641..150398617-chr6:150664104..150666636,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP1-2	chr6:150354375-150354702	NONHSAT115530
2	lnc-RAET1L-1	chr6:150361683-150362309	XLOC_005876
3	lnc-RAET1L-1	chr6:150362917-150363169	XLOC_005876
4	lnc-ULBP1-2	chr6:150353905-150354172	NONHSAT115530

No data

Variant related genes	Relation type
PHBP1	TF binding region
RAET1L	TF binding region
RAET1M	TF binding region
ENSG00000235972	TF binding region
ULBP3	TF binding region
PHBP1	CpG island
RAET1L	CpG island
RAET1M	CpG island
ENSG00000235972	CpG island
ULBP3	CpG island
ENSG00000155918	chromatin interactions
ENSG00000198729	chromatin interactions
ENSG00000213091	chromatin interactions
ENSG00000131015	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000216621	chromatin interactions
ENSG00000111981	chromatin interactions
ENSG00000218358	chromatin interactions
ENSG00000235972	chromatin interactions
ENSG00000131019	chromatin interactions
WDR11	miRNA target sites
INTS6	miRNA target sites

Extended variants
information (count: 2698 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2698 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs470448	chr6:150335407-150335408	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs543324696	chr6:150335417-150335418	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs470776	chr6:150335425-150335426	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs470775	chr6:150335431-150335432	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs556946812	chr6:150335546-150335547	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs576698637	chr6:150335595-150335596	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs545589681	chr6:150335611-150335612	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs200854765	chr6:150335627-150335628	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs564778845	chr6:150335703-150335704	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs572125348	chr6:150335760-150335761	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs372265405	chr6:150335777-150335778	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs377312607	chr6:150335781-150335782	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs144486809	chr6:150335789-150335790	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs540634396	chr6:150335798-150335799	Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs560530932	chr6:150335857-150335858	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs116362982	chr6:150335881-150335882	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs145372210	chr6:150335884-150335885	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555334403	chr6:150335905-150335906	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs549661140	chr6:150335913-150335914	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs563251832	chr6:150335922-150335923	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs537767805	chr6:150335978-150335979	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs368672018	chr6:150335983-150335984	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs117430312	chr6:150336008-150336009	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs552371234	chr6:150336020-150336021	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs571617287	chr6:150336026-150336027	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376744443	chr6:150336064-150336065	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534287113	chr6:150336068-150336069	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs547604652	chr6:150336070-150336071	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567664307	chr6:150336095-150336096	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs536688355	chr6:150336148-150336149	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369350521	chr6:150336149-150336150	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182732275	chr6:150336166-150336167	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533727810	chr6:150336174-150336175	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553632214	chr6:150336201-150336202	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185917339	chr6:150336202-150336203	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191859740	chr6:150336209-150336210	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576808811	chr6:150336211-150336212	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373422211	chr6:150336212-150336213	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538827807	chr6:150336222-150336223	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573684393	chr6:150336242-150336243	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572585266	chr6:150336296-150336297	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs541098642	chr6:150336311-150336312	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149189221	chr6:150336313-150336314	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs535928145	chr6:150336338-150336339	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556140583	chr6:150336351-150336352	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs614688	chr6:150336389-150336390	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184157874	chr6:150336397-150336398	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs3860822	chr6:150336409-150336410	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187552667	chr6:150336429-150336430	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563214854	chr6:150336464-150336465	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1365 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150330200-150336200	Weak transcription	Lung	lung
2	chr6:150335200-150336600	Bivalent Enhancer	Fetal Brain Male	brain
3	chr6:150335200-150340400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:150335400-150336800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
5	chr6:150335600-150336200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:150335600-150336600	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr6:150335800-150336000	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
8	chr6:150335800-150336000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:150335800-150336000	Bivalent Enhancer	Fetal Intestine Small	intestine
10	chr6:150335800-150336000	Bivalent/Poised TSS	Psoas Muscle	Psoas
11	chr6:150335800-150336000	Active TSS	HMEC	breast
12	chr6:150335800-150336200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:150335800-150336200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
14	chr6:150335800-150336200	Bivalent Enhancer	HUVEC	blood vessel
15	chr6:150335800-150336400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
16	chr6:150335800-150336400	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr6:150335800-150336400	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:150335800-150336400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:150335800-150336400	Bivalent Enhancer	Liver	Liver
20	chr6:150335800-150336400	Bivalent Enhancer	Fetal Stomach	stomach
21	chr6:150335800-150336600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:150335800-150336600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:150335800-150336600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:150335800-150336600	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr6:150335800-150336800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
26	chr6:150335800-150336800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
27	chr6:150335800-150336800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr6:150335800-150336800	Bivalent Enhancer	Placenta	Placenta
29	chr6:150335800-150336800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
30	chr6:150335800-150337000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr6:150336000-150336200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:150336000-150336600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
33	chr6:150336000-150336600	Enhancers	Right Atrium	heart
34	chr6:150336000-150336600	Flanking Active TSS	HMEC	breast
35	chr6:150336000-150336800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
36	chr6:150336000-150336800	Bivalent Enhancer	Esophagus	oesophagus
37	chr6:150336200-150336400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
38	chr6:150336200-150336400	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:150336200-150336400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
40	chr6:150336200-150336400	Flanking Active TSS	Right Ventricle	heart
41	chr6:150336200-150336600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
42	chr6:150336200-150336600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
43	chr6:150336200-150336600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:150336200-150336600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:150336200-150336600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:150336200-150336600	Enhancers	Pancreas	Pancrea
47	chr6:150336200-150336600	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
48	chr6:150336200-150336600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
49	chr6:150336200-150336600	Bivalent/Poised TSS	NHEK	skin
50	chr6:150336200-150336800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood

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