Variant report

Variant	esv3421775
Chromosome Location	chr1:185013354-185016202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:541)
CpG islands
(count:613)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:185014626-185014739	K562	blood:	n/a	n/a
2	ARID3A	chr1:185013996-185014669	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:185015345-185015483	K562	blood:	n/a	n/a
4	ATF3	chr1:185014449-185014848	K562	blood:	n/a	chr1:185014535-185014555 chr1:185014525-185014534
5	BACH1	chr1:185014344-185014718	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:185014945-185015477	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr1:185014176-185014703	GM12878	blood:	n/a	chr1:185014492-185014501 chr1:185014554-185014563 chr1:185014591-185014604
8	BHLHE40	chr1:185015279-185015448	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:185014351-185014745	HepG2	liver:	n/a	n/a
10	BHLHE40	chr1:185014137-185014889	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:185014062-185015702	K562	blood:	n/a	chr1:185015097-185015113
12	BRCA1	chr1:185014666-185014852	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:185015391-185015919	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr1:185013894-185015525	K562	blood:	n/a	n/a
15	CCNT2	chr1:185014274-185015281	K562	blood:	n/a	chr1:185015247-185015256 chr1:185015135-185015144 chr1:185015253-185015262
16	CEBPB	chr1:185014516-185014716	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:185014875-185014952	K562	blood:	n/a	n/a
18	CEBPB	chr1:185014545-185014729	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:185013576-185013872	K562	blood:	n/a	n/a
20	CEBPB	chr1:185015319-185015519	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:185014670-185014719	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPD	chr1:185014229-185014955	HepG2	liver:	n/a	n/a
23	CHD1	chr1:185015062-185015262	GM12878	blood:	n/a	n/a
24	CHD1	chr1:185014915-185015828	H1-hESC	embryonic stem cell:	n/a	chr1:185015452-185015462
25	CHD1	chr1:185014231-185014839	GM12878	blood:	n/a	chr1:185014523-185014533 chr1:185014792-185014802
26	CHD1	chr1:185015525-185015870	GM12878	blood:	n/a	n/a
27	CHD2	chr1:185014890-185015646	K562	blood:	n/a	chr1:185015452-185015462
28	CHD2	chr1:185014981-185015181	HepG2	liver:	n/a	n/a
29	CHD2	chr1:185014999-185015618	H1-hESC	embryonic stem cell:	n/a	chr1:185015452-185015462
30	CHD2	chr1:185014149-185015632	Hela-S3	cervix:	n/a	chr1:185014523-185014533 chr1:185014792-185014802 chr1:185015452-185015462
31	CHD2	chr1:185014306-185014670	K562	blood:	n/a	chr1:185014523-185014533
32	CHD2	chr1:185014311-185015728	GM12878	blood:	n/a	chr1:185014523-185014533 chr1:185014792-185014802 chr1:185015452-185015462
33	CHD2	chr1:185014240-185014738	H1-hESC	embryonic stem cell:	n/a	chr1:185014523-185014533
34	CHD2	chr1:185014687-185014731	HepG2	liver:	n/a	n/a
35	CREB1	chr1:185014211-185014719	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr1:185014131-185014924	A549	lung:	n/a	n/a
37	CREB1	chr1:185014173-185015164	K562	blood:	n/a	n/a
38	CREB1	chr1:185014108-185015301	GM12878	blood:	n/a	n/a
39	CREB1	chr1:185014014-185015492	HepG2	liver:	n/a	n/a
40	CTCF	chr1:185014980-185015130	SAEC	small airway:	n/a	n/a
41	CTCF	chr1:185014460-185014610	AG09319	gingival:	n/a	n/a
42	CTCF	chr1:185015240-185015390	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr1:185014364-185014618	MCF-7	breast:	n/a	chr1:185014367-185014380
44	CTCF	chr1:185014400-185014550	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:185015440-185015458	GM19240	blood:	n/a	n/a
46	CTCF	chr1:185014440-185014590	GM12871	blood:	n/a	n/a
47	CTCF	chr1:185014363-185014642	GM12892	blood:	n/a	chr1:185014367-185014380
48	CTCF	chr1:185014357-185014644	GM19239	blood:	n/a	chr1:185014367-185014380
49	CTCF	chr1:185014400-185014550	GM12874	blood:	n/a	n/a
50	CTCF	chr1:185014252-185014744	K562	blood:	n/a	chr1:185014367-185014380

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:185015449-185015499	AG09309	skin:	n/a
2	chr1:185014370-185014420	AG04449	skin:	fetal
3	chr1:185013789-185013839	AG09319	gingival:	n/a
4	chr1:185015449-185015499	AG09309	skin:	n/a
5	chr1:185014370-185014420	AG04449	skin:	fetal
6	chr1:185013789-185013839	AG09319	gingival:	n/a
7	chr1:185014370-185014420	HEEpiC	esophagus:	n/a
8	chr1:185014264-185014314	NHBE	bronchial:	n/a
9	chr1:185013789-185013839	LNCaP	prostate:	n/a
10	chr1:185015066-185015116	AoSMC	blood vessel:	n/a
11	chr1:185013789-185013839	HRCEpiC	kidney:	n/a
12	chr1:185013658-185013708	HRE	kidney:	n/a
13	chr1:185014264-185014314	SK-N-SH_RA	brain:	n/a
14	chr1:185015449-185015499	GM19239	blood:	n/a
15	chr1:185015449-185015499	IMR90	lung:	fetal
16	chr1:185013789-185013839	GM12891	blood:	n/a
17	chr1:185013789-185013839	HMEC	breast:	n/a
18	chr1:185014264-185014314	K562	blood:	n/a
19	chr1:185014181-185014231	HIPEpiC	eye:	n/a
20	chr1:185015193-185015243	SK-N-SH_RA	brain:	n/a
21	chr1:185014181-185014231	NHBE	bronchial:	n/a
22	chr1:185015449-185015499	HAEpiC	amniotic membrane:	n/a
23	chr1:185014241-185014291	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:185014370-185014420	NB4	blood:	n/a
25	chr1:185015193-185015243	ProgFib	skin:	n/a
26	chr1:185014370-185014420	AG09319	gingival:	n/a
27	chr1:185014241-185014291	MCF-7	breast:	n/a
28	chr1:185014530-185014580	HCPEpiC	choroid plexus:	n/a
29	chr1:185014181-185014231	LNCaP	prostate:	n/a
30	chr1:185014264-185014314	GM12878	blood:	n/a
31	chr1:185014241-185014291	Hela-S3	cervix:	n/a
32	chr1:185015449-185015499	ECC-1	luminal epithelium:	n/a
33	chr1:185014264-185014314	GM06990	blood:	n/a
34	chr1:185014241-185014291	H1-hESC	embryonic stem cell:	embryo
35	chr1:185014264-185014314	CMK	blood:	n/a
36	chr1:185013789-185013839	HepG2	liver:	n/a
37	chr1:185014181-185014231	BJ	skin:	n/a
38	chr1:185014370-185014420	HCT-116	colon:	n/a
39	chr1:185015449-185015499	HNPCEpiC	eye:	n/a
40	chr1:185014530-185014580	ECC-1	luminal epithelium:	n/a
41	chr1:185013658-185013708	K562	blood:	n/a
42	chr1:185014241-185014291	SAEC	small airway:	n/a
43	chr1:185015449-185015499	AoSMC	blood vessel:	n/a
44	chr1:185014264-185014314	GM12891	blood:	n/a
45	chr1:185014181-185014231	ProgFib	skin:	n/a
46	chr1:185015193-185015243	SK-N-SH	brain:	n/a
47	chr1:185014370-185014420	HRPEpiC	eye:	n/a
48	chr1:185014241-185014291	Jurkat	blood:	n/a
49	chr1:185014370-185014420	HUVEC	blood vessel:	n/a
50	chr1:185014370-185014420	K562	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:184941138..184943515-chr1:185012025..185014366,2	K562	blood:
2	chr1:185014501..185017888-chr1:185123055..185126846,5	MCF-7	breast:
3	chr1:185013842..185016800-chr1:185124120..185127493,5	MCF-7	breast:
4	chr1:185012738..185017820-chr1:185123187..185127311,9	K562	blood:
5	chr1:185014725..185016444-chr1:185285813..185288103,2	K562	blood:
6	chr1:185013977..185014692-chr17:1531841..1532366,2	Hela-S3	cervix:
7	chr1:185010844..185012522-chr1:185016130..185018992,2	MCF-7	breast:
8	chr1:184722993..184726139-chr1:185013897..185016469,4	K562	blood:
9	chr1:185010943..185013509-chr1:185124566..185127368,2	MCF-7	breast:
10	chr1:185012738..185016714-chr1:185123889..185127545,9	K562	blood:
11	chr1:185014175..185016130-chr8:128748218..128750891,2	MCF-7	breast:
12	chr1:185015280..185017121-chr1:185031346..185033713,2	MCF-7	breast:
13	chr1:185014410..185016846-chr1:185107860..185109945,2	K562	blood:
14	chr1:185016066..185017861-chr1:185027232..185029137,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNF2	TF binding region
RNF2	CpG island
ENSG00000136997	chromatin interactions
ENSG00000116668	chromatin interactions
ENSG00000121486	chromatin interactions
ENSG00000116406	chromatin interactions
ENSG00000273004	chromatin interactions
ENSG00000116679	chromatin interactions
ENSG00000167703	chromatin interactions

Extended variants
information (count: 106 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200393372	chr1:185013360-185013361	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs553998560	chr1:185013375-185013376	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs572231841	chr1:185013385-185013386	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs372033695	chr1:185013386-185013387	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs539376671	chr1:185013474-185013475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs527418411	chr1:185013475-185013476	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs557520972	chr1:185013542-185013543	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs575841792	chr1:185013586-185013587	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs571980187	chr1:185013587-185013588	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs562665938	chr1:185013638-185013639	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs181996207	chr1:185013671-185013672	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs145492610	chr1:185013679-185013680	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs549030607	chr1:185013695-185013696	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs562006054	chr1:185013708-185013709	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs560952666	chr1:185013709-185013710	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs375155697	chr1:185013724-185013725	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs185771789	chr1:185013740-185013741	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs567160487	chr1:185013759-185013760	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs189113660	chr1:185013813-185013814	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs376600496	chr1:185013818-185013819	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs181259235	chr1:185013819-185013820	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs552942410	chr1:185013838-185013839	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs186179673	chr1:185013844-185013845	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs531944099	chr1:185013951-185013952	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs549871796	chr1:185013976-185013977	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs568077247	chr1:185013981-185013982	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs535569931	chr1:185013990-185013991	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs3753573	chr1:185014002-185014003	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
29	rs549712106	chr1:185014015-185014016	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs368988154	chr1:185014021-185014022	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs372369277	chr1:185014024-185014025	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs112890078	chr1:185014082-185014083	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs369825467	chr1:185014119-185014120	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs557634593	chr1:185014154-185014155	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs575806776	chr1:185014155-185014156	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs373758464	chr1:185014206-185014207	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs191432486	chr1:185014217-185014218	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs555572935	chr1:185014227-185014228	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs574819188	chr1:185014238-185014239	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs542359348	chr1:185014277-185014278	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs74134409	chr1:185014308-185014309	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs572478222	chr1:185014321-185014322	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs571200133	chr1:185014339-185014340	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs376200603	chr1:185014357-185014358	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs374923302	chr1:185014371-185014372	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs538479407	chr1:185014389-185014390	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs531906817	chr1:185014422-185014423	Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs550381027	chr1:185014493-185014494	Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs5779238	chr1:185014506-185014507	Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs397982247	chr1:185014509-185014510	Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185010200-185014000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:185010200-185014000	Weak transcription	Fetal Muscle Leg	muscle
3	chr1:185010600-185013600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:185010600-185014000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr1:185010600-185014000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:185010600-185014000	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr1:185011000-185014000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr1:185011000-185014000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:185012200-185014000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr1:185012400-185013800	Enhancers	HepG2	liver
11	chr1:185012800-185013800	Enhancers	K562	blood
12	chr1:185012800-185014000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:185013000-185014000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr1:185013400-185014000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:185013600-185013800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr1:185013600-185013800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr1:185013600-185013800	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr1:185013600-185013800	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr1:185013600-185013800	Active TSS	Fetal Intestine Small	intestine
20	chr1:185013600-185014000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr1:185013600-185014000	Enhancers	Primary B cells from peripheral blood	blood
22	chr1:185013600-185014000	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr1:185013600-185014000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:185013600-185014000	Active TSS	Fetal Kidney	kidney
25	chr1:185013600-185014000	Enhancers	Fetal Stomach	stomach
26	chr1:185013600-185014000	Active TSS	NHDF-Ad	bronchial
27	chr1:185013600-185016000	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr1:185013600-185016200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr1:185013800-185014000	Enhancers	Primary T cells fromperipheralblood	blood
30	chr1:185013800-185014000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:185013800-185014000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr1:185013800-185014000	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr1:185013800-185014000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:185013800-185014000	Enhancers	Adipose Nuclei	Adipose
35	chr1:185013800-185014000	Enhancers	Brain Anterior Caudate	brain
36	chr1:185013800-185014000	Enhancers	A549	lung
37	chr1:185013800-185014200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr1:185013800-185014200	Flanking Active TSS	Fetal Intestine Small	intestine
39	chr1:185013800-185014200	Flanking Active TSS	HepG2	liver
40	chr1:185013800-185014400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr1:185013800-185014400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr1:185013800-185014400	Flanking Active TSS	K562	blood
43	chr1:185013800-185015400	Active TSS	Duodenum Mucosa	Duodenum
44	chr1:185013800-185015400	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr1:185013800-185015400	Active TSS	Rectal Mucosa Donor 31	rectum
46	chr1:185013800-185015600	Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr1:185013800-185015800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:185013800-185015800	Active TSS	Fetal Lung	lung
49	chr1:185013800-185016200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:185013800-185016200	Active TSS	Breast Myoepithelial Primary Cells	Breast

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