Variant report

Variant	nsv521858
Chromosome Location	chr4:2846799-2881256
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:245)
Chromatin interactive
region (count:53)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:502 , 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	chr4:2862462-2863035	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:2860145-2860576	K562	blood:	n/a	chr4:2860262-2860278
3	ARID3A	chr4:2869261-2870018	K562	blood:	n/a	chr4:2869295-2869311
4	ARID3A	chr4:2847342-2847352	K562	blood:	n/a	n/a
5	ARID3A	chr4:2867158-2867425	K562	blood:	n/a	n/a
6	ARID3A	chr4:2867618-2868034	HepG2	liver:	n/a	n/a
7	ATF1	chr4:2860232-2860557	K562	blood:	n/a	n/a
8	ATF1	chr4:2869426-2870033	K562	blood:	n/a	n/a
9	ATF2	chr4:2846931-2847503	GM12878	blood:	n/a	n/a
10	ATF2	chr4:2847014-2847432	GM12878	blood:	n/a	n/a
11	BACH1	chr4:2864493-2864719	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:2868793-2868971	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr4:2847001-2847367	GM12878	blood:	n/a	n/a
14	BATF	chr4:2847030-2847382	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:2846955-2847390	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:2847089-2847334	GM12878	blood:	n/a	n/a
17	BCLAF1	chr4:2846915-2847482	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:2854049-2854538	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:2868042-2868082	HepG2	liver:	n/a	n/a
20	BHLHE40	chr4:2860213-2860555	K562	blood:	n/a	n/a
21	BHLHE40	chr4:2854302-2854432	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:2870406-2870407	K562	blood:	n/a	n/a
23	BHLHE40	chr4:2847025-2847401	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:2869467-2870106	K562	blood:	n/a	n/a
25	BHLHE40	chr4:2849183-2849329	GM12878	blood:	n/a	n/a
26	CBX3	chr4:2859651-2860591	K562	blood:	n/a	n/a
27	CBX3	chr4:2869401-2870123	K562	blood:	n/a	n/a
28	CCNT2	chr4:2869494-2870097	K562	blood:	n/a	n/a
29	CEBPB	chr4:2860283-2860508	K562	blood:	n/a	n/a
30	CEBPB	chr4:2869449-2870113	K562	blood:	n/a	n/a
31	CEBPB	chr4:2875797-2875957	H1-hESC	embryonic stem cell:	n/a	chr4:2875893-2875904
32	CEBPB	chr4:2856740-2856891	HepG2	liver:	n/a	chr4:2856858-2856869
33	CEBPB	chr4:2869543-2870080	K562	blood:	n/a	n/a
34	CEBPB	chr4:2860110-2860679	K562	blood:	n/a	n/a
35	CEBPB	chr4:2875763-2876013	IMR90	lung:	n/a	chr4:2875893-2875904
36	CEBPB	chr4:2875753-2876060	HepG2	liver:	n/a	chr4:2875893-2875904
37	CEBPB	chr4:2875745-2876051	HepG2	liver:	n/a	chr4:2875893-2875904
38	CEBPB	chr4:2860214-2860543	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:2860135-2860589	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:2875792-2875993	HepG2	liver:	n/a	chr4:2875893-2875904
41	CEBPB	chr4:2868271-2868563	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:2860045-2860560	K562	blood:	n/a	n/a
43	CEBPD	chr4:2869328-2870235	K562	blood:	n/a	n/a
44	CEBPD	chr4:2860090-2860677	K562	blood:	n/a	n/a
45	CEBPD	chr4:2869384-2870216	K562	blood:	n/a	n/a
46	CEBPD	chr4:2860033-2860670	K562	blood:	n/a	n/a
47	CEBPD	chr4:2862745-2863060	HepG2	liver:	n/a	n/a
48	CREB1	chr4:2869457-2870176	K562	blood:	n/a	n/a
49	CREB1	chr4:2862817-2863028	A549	lung:	n/a	n/a
50	CREB1	chr4:2869330-2870148	K562	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2847213-2847263	AG09319	gingival:	n/a
2	chr4:2847213-2847263	AG09319	gingival:	n/a
3	chr4:2848840-2848890	BE2_C	brain:	n/a
4	chr4:2860776-2860826	HepG2	liver:	n/a
5	chr4:2860776-2860826	AoSMC	blood vessel:	n/a
6	chr4:2848840-2848890	ovcar-3	ovarian:	n/a
7	chr4:2869818-2869868	HAEpiC	amniotic membrane:	n/a
8	chr4:2848840-2848890	HNPCEpiC	eye:	n/a
9	chr4:2869818-2869868	SK-N-SH	brain:	n/a
10	chr4:2848840-2848890	LNCaP	prostate:	n/a
11	chr4:2848840-2848890	AoSMC	blood vessel:	n/a
12	chr4:2869818-2869868	Hela-S3	cervix:	n/a
13	chr4:2869818-2869868	GM12892	blood:	n/a
14	chr4:2860776-2860826	RPTEC	kidney:	n/a
15	chr4:2860776-2860826	GM12891	blood:	n/a
16	chr4:2848840-2848890	PrEC	prostate:	n/a
17	chr4:2847213-2847263	PrEC	prostate:	n/a
18	chr4:2847213-2847263	ProgFib	skin:	n/a
19	chr4:2860776-2860826	NB4	blood:	n/a
20	chr4:2869818-2869868	HRE	kidney:	n/a
21	chr4:2847213-2847263	BE2_C	brain:	n/a
22	chr4:2860776-2860826	HCT-116	colon:	n/a
23	chr4:2848840-2848890	AG04449	skin:	fetal
24	chr4:2860776-2860826	SK-N-SH_RA	brain:	n/a
25	chr4:2847213-2847263	GM19239	blood:	n/a
26	chr4:2869818-2869868	K562	blood:	n/a
27	chr4:2848840-2848890	SK-N-SH	brain:	n/a
28	chr4:2860776-2860826	AG04450	lung:	fetal
29	chr4:2847213-2847263	NHDF-neo	bronchial:	n/a
30	chr4:2860776-2860826	NH-A	brain:	n/a
31	chr4:2848840-2848890	GM12891	blood:	n/a
32	chr4:2869818-2869868	HRCEpiC	kidney:	n/a
33	chr4:2847213-2847263	GM12878	blood:	n/a
34	chr4:2848840-2848890	PANC-1	pancreas:	n/a
35	chr4:2848840-2848890	U87	brain:	n/a
36	chr4:2848840-2848890	HEK293	kidney:	embryo
37	chr4:2869818-2869868	HepG2	liver:	n/a
38	chr4:2847213-2847263	HRE	kidney:	n/a
39	chr4:2848840-2848890	AG09319	gingival:	n/a
40	chr4:2860776-2860826	BJ	skin:	n/a
41	chr4:2848840-2848890	Hela-S3	cervix:	n/a
42	chr4:2860776-2860826	HL-60	blood:	n/a
43	chr4:2860776-2860826	AG04449	skin:	fetal
44	chr4:2860776-2860826	SK-N-MC	brain:	n/a
45	chr4:2848840-2848890	NT2-D1	testis:	n/a
46	chr4:2848840-2848890	MCF10A-Er-Src	breast:	n/a
47	chr4:2847213-2847263	HCF	heart:	n/a
48	chr4:2848840-2848890	HCM	heart:	n/a
49	chr4:2847213-2847263	NHBE	bronchial:	n/a
50	chr4:2860776-2860826	HRE	kidney:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:2864305..2866761-chr4:2868243..2869773,2	K562	blood:
2	chr4:2866369..2868735-chr4:2871007..2873229,2	MCF-7	breast:
3	chr4:2865723..2868590-chr4:2936082..2937695,2	MCF-7	breast:
4	chr4:2848510..2850735-chr4:2868206..2870939,2	K562	blood:
5	chr4:2873606..2876373-chr4:2925507..2927684,2	MCF-7	breast:
6	chr4:2844665..2847425-chr4:2860428..2864789,5	MCF-7	breast:
7	chr4:2855740..2858209-chr4:2858751..2860482,2	K562	blood:
8	chr4:2867681..2870567-chr4:2936383..2939288,2	MCF-7	breast:
9	chr4:2859689..2861245-chr4:2862909..2865394,2	MCF-7	breast:
10	chr4:2857762..2859404-chr4:2861452..2863344,2	MCF-7	breast:
11	chr4:2867163..2870465-chr4:2873616..2875440,4	K562	blood:
12	chr4:2847502..2850014-chr4:2935362..2937925,4	MCF-7	breast:
13	chr4:2846050..2847976-chr4:2912063..2913866,2	MCF-7	breast:
14	chr4:2876464..2878755-chr4:2882679..2884281,2	K562	blood:
15	chr4:2843889..2847586-chr4:2849028..2855037,6	K562	blood:
16	chr4:2795244..2797486-chr4:2845439..2847269,2	MCF-7	breast:
17	chr4:2858420..2861914-chr4:2865783..2871462,7	K562	blood:
18	chr4:2845404..2847784-chr4:2938194..2940916,3	MCF-7	breast:
19	chr4:2804665..2806753-chr4:2851605..2853395,2	MCF-7	breast:
20	chr4:2819892..2821779-chr4:2853270..2855073,2	MCF-7	breast:
21	chr4:2866956..2870306-chr4:2932983..2937533,4	K562	blood:
22	chr4:2844708..2848266-chr4:2857886..2861827,4	K562	blood:
23	chr4:2879534..2882793-chr4:2935370..2940285,4	MCF-7	breast:
24	chr4:2756622..2759640-chr4:2845812..2847874,4	MCF-7	breast:
25	chr4:2844179..2847079-chr4:2935598..2937938,4	MCF-7	breast:
26	chr4:2846265..2848875-chr4:2873594..2875378,2	K562	blood:
27	chr4:2855341..2858315-chr4:2935063..2937111,2	MCF-7	breast:
28	chr4:2871630..2873574-chr4:2881576..2884568,2	K562	blood:
29	chr4:2818404..2821312-chr4:2845258..2848491,3	MCF-7	breast:
30	chr4:2824402..2830718-chr4:2842859..2847645,11	MCF-7	breast:
31	chr4:2871947..2873673-chr4:2935533..2937298,2	MCF-7	breast:
32	chr4:2845095..2847586-chr4:2852811..2854373,2	K562	blood:
33	chr4:2857762..2859404-chr4:2861452..2863344,2	MCF-7	breast:
34	chr4:2845175..2847151-chr4:2963481..2966387,2	MCF-7	breast:
35	chr4:2860130..2862463-chr4:2876073..2878049,2	K562	blood:
36	chr4:2821326..2822981-chr4:2847695..2849369,2	MCF-7	breast:
37	chr4:2859689..2861245-chr4:2862909..2865394,2	MCF-7	breast:
38	chr4:2872526..2874787-chr4:2876433..2878036,2	K562	blood:
39	chr4:2846265..2848875-chr4:2873594..2875378,2	K562	blood:
40	chr4:2866369..2868735-chr4:2871007..2873229,2	MCF-7	breast:
41	chr4:2844628..2846821-chr4:2925950..2928753,2	MCF-7	breast:
42	chr4:2757710..2760448-chr4:2844046..2847029,2	K562	blood:
43	chr4:2876022..2879054-chr4:2934409..2936795,3	MCF-7	breast:
44	chr4:2794525..2804465-chr4:2841103..2847851,19	MCF-7	breast:
45	chr4:2843889..2847586-chr4:2849028..2855037,6	K562	blood:
46	chr4:2868702..2870783-chr4:2881589..2883580,3	K562	blood:
47	chr4:2858420..2863571-chr4:2865919..2871146,8	K562	blood:
48	chr2:226959307..226961604-chr4:2869808..2871481,2	MCF-7	breast:
49	chr4:2843310..2847623-chr4:2847879..2851865,7	K562	blood:
50	chr4:2855740..2858209-chr4:2858751..2860482,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3BP2-4	chr4:2878773-2878996	expReg_chr4_474_+
2	lnc-SH3BP2-2	chr4:2855351-2855425	NONHSAT094815
3	lnc-SH3BP2-2	chr4:2856581-2856677	NONHSAT094813
4	lnc-SH3BP2-2	chr4:2856581-2856756	NONHSAT094815
5	lnc-SH3BP2-2	chr4:2869699-2869822	NONHSAT094815
6	lnc-SH3BP2-2	chr4:2854861-2854930	NONHSAT094815
7	lnc-SH3BP2-3	chr4:2878344-2878589	expReg_chr4_472_+
8	lnc-SH3BP2-2	chr4:2855351-2855425	NONHSAT094813

No data

Variant related genes	Relation type
ADD1	TF binding region
ADD1	CpG island
ENSG00000125388	chromatin interactions
ENSG00000087274	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000087269	chromatin interactions
ENSG00000168884	chromatin interactions
ENSG00000087266	chromatin interactions
ENSG00000249673	chromatin interactions

Extended variants
information (count: 1310 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1310 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1877723	chr4:2846799-2846800	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556572785	chr4:2846808-2846809	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs59579107	chr4:2846809-2846810	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs397945344	chr4:2846818-2846819	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs527873805	chr4:2846835-2846836	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs184396807	chr4:2846850-2846851	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs540347749	chr4:2846853-2846854	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs375516210	chr4:2846857-2846858	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs187252514	chr4:2846865-2846866	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs532136573	chr4:2846872-2846873	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs370273641	chr4:2846903-2846904	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs568826376	chr4:2846944-2846945	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs531553307	chr4:2846960-2846961	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs548058061	chr4:2846965-2846966	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs567947920	chr4:2846973-2846974	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs533703838	chr4:2847015-2847016	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs553867843	chr4:2847030-2847031	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs374057385	chr4:2847044-2847045	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs191870072	chr4:2847045-2847046	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs539828792	chr4:2847100-2847101	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs548554684	chr4:2847160-2847161	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs150312592	chr4:2847225-2847226	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs576365548	chr4:2847230-2847231	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs542194488	chr4:2847238-2847239	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs112099864	chr4:2847266-2847267	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs78188509	chr4:2847304-2847305	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs572702270	chr4:2847372-2847373	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs16843451	chr4:2847578-2847579	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560298780	chr4:2847583-2847584	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs137984267	chr4:2847608-2847609	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs537516748	chr4:2847666-2847667	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs556118965	chr4:2847669-2847670	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs571397206	chr4:2847686-2847687	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs184095880	chr4:2847705-2847706	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs546869942	chr4:2847760-2847761	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs562371281	chr4:2847768-2847769	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs142415735	chr4:2847782-2847783	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs116649293	chr4:2847806-2847807	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs140732774	chr4:2847819-2847820	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs373740516	chr4:2847822-2847823	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs548095242	chr4:2847829-2847830	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs114213603	chr4:2847857-2847858	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs188431250	chr4:2847860-2847861	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs547147213	chr4:2847878-2847879	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs556534212	chr4:2847880-2847881	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs571963554	chr4:2847901-2847902	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs535867668	chr4:2847916-2847917	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs556607165	chr4:2847917-2847918	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs79851133	chr4:2847956-2847957	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs75957797	chr4:2848029-2848030	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Ependymoma	20639864	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2512 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2844400-2846800	Active TSS	H9 Cell Line	embryonic stem cell
2	chr4:2844600-2846800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:2844600-2847000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:2844600-2847400	Active TSS	Brain Angular Gyrus	brain
5	chr4:2844600-2847400	Active TSS	Brain Inferior Temporal Lobe	brain
6	chr4:2844600-2847400	Active TSS	Ovary	ovary
7	chr4:2844800-2846800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:2844800-2846800	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr4:2844800-2846800	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr4:2844800-2846800	Active TSS	Aorta	Aorta
11	chr4:2844800-2847000	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr4:2844800-2847000	Active TSS	Gastric	stomach
13	chr4:2844800-2847200	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr4:2844800-2847200	Active TSS	Brain Cingulate Gyrus	brain
15	chr4:2844800-2847200	Active TSS	Small Intestine	intestine
16	chr4:2844800-2847200	Active TSS	HSMM	muscle
17	chr4:2844800-2847400	Active TSS	Psoas Muscle	Psoas
18	chr4:2844800-2847400	Active TSS	Right Ventricle	heart
19	chr4:2844800-2847400	Active TSS	NHDF-Ad	bronchial
20	chr4:2844800-2847600	Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr4:2844800-2847800	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr4:2845000-2846800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:2845000-2846800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr4:2845000-2846800	Active TSS	Brain Substantia Nigra	brain
25	chr4:2845000-2846800	Active TSS	Esophagus	oesophagus
26	chr4:2845000-2846800	Active TSS	Fetal Intestine Large	intestine
27	chr4:2845000-2846800	Active TSS	Fetal Stomach	stomach
28	chr4:2845000-2846800	Active TSS	Lung	lung
29	chr4:2845000-2846800	Active TSS	Spleen	Spleen
30	chr4:2845000-2847000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:2845000-2847000	Active TSS	Muscle Satellite Cultured Cells	--
32	chr4:2845000-2847000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr4:2845000-2847000	Active TSS	Colonic Mucosa	Colon
34	chr4:2845000-2847200	Active TSS	Brain Hippocampus Middle	brain
35	chr4:2845000-2847200	Active TSS	Fetal Brain Female	brain
36	chr4:2845000-2847200	Active TSS	A549	lung
37	chr4:2845000-2847400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:2845000-2847400	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr4:2845000-2847400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:2845000-2847400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:2845000-2847400	Active TSS	Stomach Smooth Muscle	stomach
42	chr4:2845000-2847400	Active TSS	GM12878-XiMat	blood
43	chr4:2845000-2847400	Active TSS	HSMMtube	muscle
44	chr4:2845000-2847400	Active TSS	NHLF	lung
45	chr4:2845000-2847600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:2845000-2847600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:2845000-2847800	Active TSS	K562	blood
48	chr4:2845000-2848200	Active TSS	Brain Germinal Matrix	brain
49	chr4:2845200-2846800	Active TSS	Fetal Muscle Trunk	muscle
50	chr4:2845200-2846800	Active TSS	Placenta	Placenta

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