Variant report

Variant	nsv1013076
Chromosome Location	chr1:180214152-180239670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:962)
CpG islands
(count:183)
Chromatin interactive
region (count:66)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:962 , 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	chr1:180222982-180223054	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:180216819-180217020	HepG2	liver:	n/a	n/a
3	ATF2	chr1:180221751-180222128	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:180239290-180239643	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr1:180218789-180219248	GM12878	blood:	n/a	chr1:180219150-180219163
6	BCL3	chr1:180218839-180219180	GM12878	blood:	n/a	chr1:180219150-180219163
7	BCLAF1	chr1:180221737-180222125	GM12878	blood:	n/a	chr1:180221897-180221906
8	BCLAF1	chr1:180221705-180222139	GM12878	blood:	n/a	chr1:180221897-180221906
9	BHLHE40	chr1:180224732-180224982	K562	blood:	n/a	n/a
10	BHLHE40	chr1:180239124-180239134	K562	blood:	n/a	n/a
11	BHLHE40	chr1:180221827-180222085	K562	blood:	n/a	n/a
12	BHLHE40	chr1:180221898-180222113	HepG2	liver:	n/a	n/a
13	BRCA1	chr1:180222972-180222994	HepG2	liver:	n/a	n/a
14	BRCA1	chr1:180239398-180239598	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr1:180221711-180222198	K562	blood:	n/a	n/a
16	CBX3	chr1:180218440-180218762	K562	blood:	n/a	n/a
17	CEBPB	chr1:180221728-180222237	MCF-7	breast:	n/a	chr1:180221759-180221770
18	CEBPB	chr1:180221803-180222190	K562	blood:	n/a	n/a
19	CEBPB	chr1:180221797-180222194	A549	lung:	n/a	n/a
20	CEBPB	chr1:180221878-180222083	K562	blood:	n/a	n/a
21	CEBPB	chr1:180238784-180238935	K562	blood:	n/a	n/a
22	CEBPB	chr1:180221799-180222171	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:180218012-180218194	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:180221776-180222171	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:180238827-180238939	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:180221806-180222151	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:180216211-180216475	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:180221801-180222155	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:180221690-180222180	A549	lung:	n/a	chr1:180221759-180221770
30	CEBPB	chr1:180221735-180222154	K562	blood:	n/a	chr1:180221759-180221770
31	CHD2	chr1:180223296-180223709	HepG2	liver:	n/a	n/a
32	CHD2	chr1:180217376-180217539	HepG2	liver:	n/a	n/a
33	CHD2	chr1:180229863-180229865	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr1:180239264-180239534	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr1:180239305-180239323	HepG2	liver:	n/a	n/a
36	CTBP2	chr1:180213745-180214464	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr1:180218600-180218750	GM12864	blood:	n/a	chr1:180218644-180218654
38	CTCF	chr1:180221880-180222030	GM12871	blood:	n/a	chr1:180221941-180221959 chr1:180221946-180221956 chr1:180221943-180221964
39	CTCF	chr1:180239500-180239650	AG04450	lung:	n/a	n/a
40	CTCF	chr1:180239164-180239231	NHEK	skin:	n/a	n/a
41	CTCF	chr1:180239480-180239630	AG04449	skin:	n/a	n/a
42	CTCF	chr1:180239440-180239590	HMEC	breast:	n/a	n/a
43	CTCF	chr1:180218620-180218770	GM12873	blood:	n/a	chr1:180218644-180218654
44	CTCF	chr1:180221545-180222181	GM12878	blood:	n/a	chr1:180221941-180221959 chr1:180221946-180221956 chr1:180221943-180221964
45	CTCF	chr1:180218560-180218710	GM12864	blood:	n/a	chr1:180218644-180218654
46	CTCF	chr1:180228553-180228611	GM19238	blood:	n/a	n/a
47	CTCF	chr1:180239429-180239664	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:180218500-180218650	GM12870	blood:	n/a	n/a
49	CTCF	chr1:180221860-180222010	HCT-116	colon:	n/a	chr1:180221941-180221959 chr1:180221946-180221956 chr1:180221943-180221964
50	CTCF	chr1:180221880-180222030	HMF	breast:	n/a	chr1:180221941-180221959 chr1:180221946-180221956 chr1:180221943-180221964

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180236510-180236560	Caco-2	colon:	n/a
2	chr1:180224709-180224759	ProgFib	skin:	n/a
3	chr1:180224709-180224759	HEEpiC	esophagus:	n/a
4	chr1:180224709-180224759	PFSK-1	brain:	n/a
5	chr1:180236510-180236560	Jurkat	blood:	n/a
6	chr1:180218208-180218258	HCM	heart:	n/a
7	chr1:180218208-180218258	Jurkat	blood:	n/a
8	chr1:180224709-180224759	GM06990	blood:	n/a
9	chr1:180224709-180224759	HMEC	breast:	n/a
10	chr1:180224709-180224759	HNPCEpiC	eye:	n/a
11	chr1:180236510-180236560	HRCEpiC	kidney:	n/a
12	chr1:180236510-180236560	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:180236510-180236560	GM12891	blood:	n/a
14	chr1:180218208-180218258	GM19239	blood:	n/a
15	chr1:180236510-180236560	Hepatocyte	liver:	n/a
16	chr1:180236510-180236560	HUVEC	blood vessel:	n/a
17	chr1:180218208-180218258	NHDF-neo	bronchial:	n/a
18	chr1:180236510-180236560	U87	brain:	n/a
19	chr1:180218208-180218258	RPTEC	kidney:	n/a
20	chr1:180218208-180218258	HIPEpiC	eye:	n/a
21	chr1:180224709-180224759	GM12891	blood:	n/a
22	chr1:180224709-180224759	HAEpiC	amniotic membrane:	n/a
23	chr1:180218208-180218258	HRCEpiC	kidney:	n/a
24	chr1:180218208-180218258	HNPCEpiC	eye:	n/a
25	chr1:180236510-180236560	AG09309	skin:	n/a
26	chr1:180236510-180236560	HEK293	kidney:	embryo
27	chr1:180224709-180224759	Hepatocyte	liver:	n/a
28	chr1:180236510-180236560	NHBE	bronchial:	n/a
29	chr1:180224709-180224759	AG04450	lung:	fetal
30	chr1:180236510-180236560	HCT-116	colon:	n/a
31	chr1:180236510-180236560	ovcar-3	ovarian:	n/a
32	chr1:180218208-180218258	K562	blood:	n/a
33	chr1:180218208-180218258	U87	brain:	n/a
34	chr1:180218208-180218258	T-47D	breast:	n/a
35	chr1:180218208-180218258	HAEpiC	amniotic membrane:	n/a
36	chr1:180236510-180236560	NH-A	brain:	n/a
37	chr1:180218208-180218258	ovcar-3	ovarian:	n/a
38	chr1:180218208-180218258	HCT-116	colon:	n/a
39	chr1:180218208-180218258	GM12892	blood:	n/a
40	chr1:180218208-180218258	GM12878	blood:	n/a
41	chr1:180236510-180236560	ProgFib	skin:	n/a
42	chr1:180236510-180236560	SAEC	small airway:	n/a
43	chr1:180218208-180218258	ECC-1	luminal epithelium:	n/a
44	chr1:180236510-180236560	HRPEpiC	eye:	n/a
45	chr1:180224709-180224759	RPTEC	kidney:	n/a
46	chr1:180224709-180224759	HCT-116	colon:	n/a
47	chr1:180236510-180236560	LNCaP	prostate:	n/a
48	chr1:180224709-180224759	AG04449	skin:	fetal
49	chr1:180236510-180236560	HCM	heart:	n/a
50	chr1:180218208-180218258	SK-N-SH_RA	brain:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:180197810..180199929-chr1:180225212..180227754,2	MCF-7	breast:
2	chr1:180221876..180222417-chr1:180451282..180451839,4	K562	blood:
3	chr1:180226912..180229884-chr1:180233692..180235253,2	K562	blood:
4	chr1:180228697..180230849-chr1:180243270..180244817,2	K562	blood:
5	chr1:180219285..180221814-chr1:180225122..180228087,3	K562	blood:
6	chr1:180221460..180222513-chr1:180446948..180447843,5	K562	blood:
7	chr1:180221695..180222356-chr1:180382040..180383006,2	MCF-7	breast:
8	chr1:180221132..180228794-chr1:180228825..180237340,13	K562	blood:
9	chr1:180224817..180227850-chr1:180239195..180241654,3	MCF-7	breast:
10	chr1:180197410..180201386-chr1:180231377..180237159,7	MCF-7	breast:
11	chr1:180197757..180200322-chr1:180217302..180220148,2	K562	blood:
12	chr1:180198334..180202186-chr1:180213057..180215883,3	K562	blood:
13	chr1:180226218..180228794-chr1:180228958..180230849,2	K562	blood:
14	chr1:180155464..180157247-chr1:180221856..180223365,2	K562	blood:
15	chr1:180213073..180215826-chr1:180222774..180224846,2	K562	blood:
16	chr1:180221615..180222392-chr1:180451323..180452198,2	MCF-7	breast:
17	chr1:180226912..180229884-chr1:180233692..180235253,2	K562	blood:
18	chr1:180216843..180220408-chr1:180221567..180224092,3	K562	blood:
19	chr1:180221132..180228794-chr1:180228825..180237340,13	K562	blood:
20	chr1:180224667..180226177-chr1:180228800..180230829,2	K562	blood:
21	chr1:180239508..180240426-chr1:180333226..180333972,2	MCF-7	breast:
22	chr1:180226218..180228794-chr1:180228958..180230849,2	K562	blood:
23	chr1:180198334..180201328-chr1:180213324..180215883,2	K562	blood:
24	chr1:180226862..180229211-chr1:180475733..180477754,2	MCF-7	breast:
25	chr1:180200127..180202190-chr1:180221742..180224179,2	MCF-7	breast:
26	chr1:180223698..180225799-chr1:180234216..180237340,3	K562	blood:
27	chr1:180223698..180225799-chr1:180234216..180237340,3	K562	blood:
28	chr1:180221964..180223660-chr1:180469973..180471619,2	MCF-7	breast:
29	chr1:180200237..180200800-chr1:180221493..180222077,2	MCF-7	breast:
30	chr1:180239113..180241283-chr1:180242753..180244604,3	MCF-7	breast:
31	chr1:180239151..180242190-chr1:180245057..180248684,4	MCF-7	breast:
32	chr1:180197450..180200103-chr1:180218151..180221090,2	MCF-7	breast:
33	chr1:180199812..180202263-chr1:180239258..180241865,2	MCF-7	breast:
34	chr1:180220889..180223156-chr1:180225392..180228382,2	K562	blood:
35	chr1:180198631..180200637-chr1:180221908..180224237,2	K562	blood:
36	chr1:180199210..180201909-chr1:180224032..180226440,2	MCF-7	breast:
37	chr1:180229024..180231831-chr1:180234327..180236591,2	K562	blood:
38	chr1:180221502..180222361-chr1:180447062..180448015,4	MCF-7	breast:
39	chr1:180219285..180221814-chr1:180225122..180228087,3	K562	blood:
40	chr1:180213073..180215826-chr1:180222774..180224846,2	K562	blood:
41	chr1:180199784..180201302-chr1:180212906..180214774,2	MCF-7	breast:
42	chr1:180222481..180224218-chr1:180470814..180473381,2	K562	blood:
43	chr1:180234099..180236359-chr1:180237257..180239459,3	MCF-7	breast:
44	chr1:180188180..180191115-chr1:180220130..180223049,2	K562	blood:
45	chr1:180221010..180222431-chr1:180384882..180385873,4	MCF-7	breast:
46	chr1:180194875..180197086-chr1:180228281..180230421,3	MCF-7	breast:
47	chr1:180222556..180224240-chr1:180362387..180364458,2	MCF-7	breast:
48	chr1:180220917..180222476-chr1:180232380..180234060,2	MCF-7	breast:
49	chr1:180221511..180222402-chr1:180384611..180385850,8	K562	blood:
50	chr1:180236987..180238620-chr1:180240813..180243453,2	K562	blood:

No data

Variant related genes	Relation type
LHX4	TF binding region
LHX4	CpG island
ENSG00000135847	chromatin interactions
ENSG00000230124	chromatin interactions
ENSG00000121454	chromatin interactions

Extended variants
information (count: 1136 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371930327	chr1:180214208-180214209	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs6673375	chr1:180214213-180214214	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563156061	chr1:180214275-180214276	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs3911336	chr1:180214353-180214354	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs545884125	chr1:180214357-180214358	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559228308	chr1:180214381-180214382	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs533834734	chr1:180214416-180214417	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs548241538	chr1:180214424-180214425	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs3911335	chr1:180214469-180214470	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs561551572	chr1:180214528-180214529	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530439382	chr1:180214536-180214537	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs539141591	chr1:180214618-180214619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs371626035	chr1:180214651-180214652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570242113	chr1:180214659-180214660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538811564	chr1:180214660-180214661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374782130	chr1:180214670-180214671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538569737	chr1:180214674-180214675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547354383	chr1:180214727-180214728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566083812	chr1:180214746-180214747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559142977	chr1:180214751-180214752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs549305220	chr1:180214755-180214756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368839261	chr1:180214840-180214841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371723080	chr1:180214918-180214919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373641115	chr1:180214939-180214940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374642118	chr1:180214940-180214941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75898070	chr1:180214958-180214959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs146717281	chr1:180214974-180214975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140315324	chr1:180215003-180215004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150418621	chr1:180215068-180215069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12135955	chr1:180215116-180215117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545727152	chr1:180215128-180215129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113141170	chr1:180215142-180215143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75537949	chr1:180215143-180215144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs58638651	chr1:180215150-180215151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs375354459	chr1:180215154-180215155	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs76687849	chr1:180215166-180215167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs182373023	chr1:180215197-180215198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186986330	chr1:180215211-180215212	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191062746	chr1:180215222-180215223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369942135	chr1:180215270-180215271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs116306288	chr1:180215271-180215272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373122679	chr1:180215339-180215340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs570292311	chr1:180215394-180215395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185405308	chr1:180215419-180215420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377275392	chr1:180215435-180215436	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559269919	chr1:180215457-180215458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552523094	chr1:180215463-180215464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577583582	chr1:180215491-180215492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566245653	chr1:180215527-180215528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553910921	chr1:180215573-180215574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
Chordoma	18071362	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD

Chromatin state (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180209000-180214800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:180210600-180214200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:180211200-180214400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:180211800-180216400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr1:180212600-180216200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr1:180213000-180215800	Weak transcription	A549	lung
7	chr1:180213600-180214200	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr1:180213600-180225800	Weak transcription	Right Atrium	heart
9	chr1:180213800-180214200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr1:180213800-180214400	Enhancers	Duodenum Mucosa	Duodenum
11	chr1:180213800-180214600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:180213800-180214600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr1:180214000-180214200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr1:180214000-180214200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:180214000-180214200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr1:180214000-180214200	Bivalent Enhancer	Fetal Intestine Large	intestine
17	chr1:180214000-180214400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr1:180214000-180214400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr1:180214000-180214600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr1:180214000-180214600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr1:180214000-180214600	Bivalent Enhancer	Colonic Mucosa	Colon
22	chr1:180214000-180214600	Flanking Active TSS	HepG2	liver
23	chr1:180214200-180214400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:180214200-180214400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr1:180214200-180214400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:180214200-180214400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
27	chr1:180214200-180216200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr1:180214200-180216400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr1:180214400-180214600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:180214400-180216000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr1:180214400-180216200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:180214400-180216400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:180214400-180216800	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:180214400-180217200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr1:180214600-180216000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr1:180214600-180216200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr1:180214600-180216200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr1:180214600-180216800	Enhancers	HepG2	liver
39	chr1:180214800-180216800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:180215200-180216000	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr1:180215800-180216400	Enhancers	A549	lung
42	chr1:180215800-180216800	Enhancers	Hela-S3	cervix
43	chr1:180216000-180216600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr1:180216000-180216800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr1:180216000-180216800	Enhancers	GM12878-XiMat	blood
46	chr1:180216000-180217000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr1:180216000-180217000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:180216000-180217400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr1:180216200-180216800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:180216200-180217000	Enhancers	HUES6 Cell Line	embryonic stem cell

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