Variant report

Variant	nsv524060
Chromosome Location	chr4:2850142-2881256
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:430)
CpG islands
(count:122)
Chromatin interactive
region (count:38)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:2869261-2870018	K562	blood:	n/a	chr4:2869295-2869311
2	ARID3A	chr4:2860145-2860576	K562	blood:	n/a	chr4:2860262-2860278
3	ARID3A	chr4:2862462-2863035	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:2867158-2867425	K562	blood:	n/a	n/a
5	ARID3A	chr4:2867618-2868034	HepG2	liver:	n/a	n/a
6	ATF1	chr4:2860232-2860557	K562	blood:	n/a	n/a
7	ATF1	chr4:2869426-2870033	K562	blood:	n/a	n/a
8	BACH1	chr4:2864493-2864719	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:2868793-2868971	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr4:2854049-2854538	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:2860213-2860555	K562	blood:	n/a	n/a
12	BHLHE40	chr4:2870406-2870407	K562	blood:	n/a	n/a
13	BHLHE40	chr4:2869467-2870106	K562	blood:	n/a	n/a
14	BHLHE40	chr4:2854302-2854432	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:2868042-2868082	HepG2	liver:	n/a	n/a
16	CBX3	chr4:2859651-2860591	K562	blood:	n/a	n/a
17	CBX3	chr4:2869401-2870123	K562	blood:	n/a	n/a
18	CCNT2	chr4:2869494-2870097	K562	blood:	n/a	n/a
19	CEBPB	chr4:2875753-2876060	HepG2	liver:	n/a	chr4:2875893-2875904
20	CEBPB	chr4:2869449-2870113	K562	blood:	n/a	n/a
21	CEBPB	chr4:2860045-2860560	K562	blood:	n/a	n/a
22	CEBPB	chr4:2860110-2860679	K562	blood:	n/a	n/a
23	CEBPB	chr4:2875763-2876013	IMR90	lung:	n/a	chr4:2875893-2875904
24	CEBPB	chr4:2875797-2875957	H1-hESC	embryonic stem cell:	n/a	chr4:2875893-2875904
25	CEBPB	chr4:2869543-2870080	K562	blood:	n/a	n/a
26	CEBPB	chr4:2860283-2860508	K562	blood:	n/a	n/a
27	CEBPB	chr4:2875792-2875993	HepG2	liver:	n/a	chr4:2875893-2875904
28	CEBPB	chr4:2868271-2868563	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:2856740-2856891	HepG2	liver:	n/a	chr4:2856858-2856869
30	CEBPB	chr4:2860214-2860543	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:2860135-2860589	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:2875745-2876051	HepG2	liver:	n/a	chr4:2875893-2875904
33	CEBPD	chr4:2869384-2870216	K562	blood:	n/a	n/a
34	CEBPD	chr4:2869328-2870235	K562	blood:	n/a	n/a
35	CEBPD	chr4:2862745-2863060	HepG2	liver:	n/a	n/a
36	CEBPD	chr4:2860033-2860670	K562	blood:	n/a	n/a
37	CEBPD	chr4:2860090-2860677	K562	blood:	n/a	n/a
38	CREB1	chr4:2869330-2870148	K562	blood:	n/a	n/a
39	CREB1	chr4:2869457-2870176	K562	blood:	n/a	n/a
40	CREB1	chr4:2862817-2863028	A549	lung:	n/a	n/a
41	CTCF	chr4:2875860-2876010	AG04450	lung:	n/a	n/a
42	CTCF	chr4:2851460-2851610	AG09319	gingival:	n/a	n/a
43	CTCF	chr4:2851396-2851534	HepG2	liver:	n/a	n/a
44	CTCF	chr4:2869860-2870010	HCPEpiC	choroid plexus:	n/a	chr4:2869974-2869987
45	CTCF	chr4:2851435-2851571	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:2851400-2851550	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr4:2851500-2851650	AG10803	skin:	n/a	n/a
48	CTCF	chr4:2850580-2850730	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr4:2869940-2870090	HPF	lung:	n/a	chr4:2869974-2869987
50	CTCF	chr4:2854140-2854290	GM12873	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2869818-2869868	AG04450	lung:	fetal
2	chr4:2869818-2869868	Jurkat	blood:	n/a
3	chr4:2860776-2860826	HEK293	kidney:	embryo
4	chr4:2869818-2869868	SKMC	muscle:	n/a
5	chr4:2860776-2860826	HMEC	breast:	n/a
6	chr4:2860776-2860826	IMR90	lung:	fetal
7	chr4:2869818-2869868	HCT-116	colon:	n/a
8	chr4:2869818-2869868	Hepatocyte	liver:	n/a
9	chr4:2869818-2869868	ovcar-3	ovarian:	n/a
10	chr4:2860776-2860826	GM12878	blood:	n/a
11	chr4:2860776-2860826	GM12892	blood:	n/a
12	chr4:2869818-2869868	HepG2	liver:	n/a
13	chr4:2860776-2860826	MCF-7	breast:	n/a
14	chr4:2869818-2869868	MCF10A-Er-Src	breast:	n/a
15	chr4:2869818-2869868	Caco-2	colon:	n/a
16	chr4:2869818-2869868	MCF-7	breast:	n/a
17	chr4:2860776-2860826	AoSMC	blood vessel:	n/a
18	chr4:2869818-2869868	HNPCEpiC	eye:	n/a
19	chr4:2869818-2869868	HRPEpiC	eye:	n/a
20	chr4:2860776-2860826	AG09319	gingival:	n/a
21	chr4:2860776-2860826	GM12891	blood:	n/a
22	chr4:2869818-2869868	NB4	blood:	n/a
23	chr4:2869818-2869868	K562	blood:	n/a
24	chr4:2869818-2869868	SK-N-MC	brain:	n/a
25	chr4:2869818-2869868	BE2_C	brain:	n/a
26	chr4:2869818-2869868	BJ	skin:	n/a
27	chr4:2860776-2860826	NH-A	brain:	n/a
28	chr4:2860776-2860826	SKMC	muscle:	n/a
29	chr4:2869818-2869868	HAEpiC	amniotic membrane:	n/a
30	chr4:2860776-2860826	ProgFib	skin:	n/a
31	chr4:2860776-2860826	Jurkat	blood:	n/a
32	chr4:2869818-2869868	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:2869818-2869868	CMK	blood:	n/a
34	chr4:2869818-2869868	NHBE	bronchial:	n/a
35	chr4:2869818-2869868	GM12891	blood:	n/a
36	chr4:2860776-2860826	HRCEpiC	kidney:	n/a
37	chr4:2869818-2869868	A549	lung:	n/a
38	chr4:2860776-2860826	Hela-S3	cervix:	n/a
39	chr4:2869818-2869868	HMEC	breast:	n/a
40	chr4:2860776-2860826	CMK	blood:	n/a
41	chr4:2869818-2869868	AG10803	skin:	n/a
42	chr4:2869818-2869868	U87	brain:	n/a
43	chr4:2869818-2869868	LNCaP	prostate:	n/a
44	chr4:2860776-2860826	ovcar-3	ovarian:	n/a
45	chr4:2869818-2869868	GM12892	blood:	n/a
46	chr4:2860776-2860826	GM06990	blood:	n/a
47	chr4:2869818-2869868	T-47D	breast:	n/a
48	chr4:2869818-2869868	AG09319	gingival:	n/a
49	chr4:2860776-2860826	NHBE	bronchial:	n/a
50	chr4:2860776-2860826	HEEpiC	esophagus:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2844665..2847425-chr4:2860428..2864789,5	MCF-7	breast:
2	chr4:2879534..2882793-chr4:2935370..2940285,4	MCF-7	breast:
3	chr4:2857762..2859404-chr4:2861452..2863344,2	MCF-7	breast:
4	chr4:2871630..2873574-chr4:2881576..2884568,2	K562	blood:
5	chr4:2858420..2861914-chr4:2865783..2871462,7	K562	blood:
6	chr4:2843889..2847586-chr4:2849028..2855037,6	K562	blood:
7	chr4:2865723..2868590-chr4:2936082..2937695,2	MCF-7	breast:
8	chr4:2843310..2847623-chr4:2847879..2851865,7	K562	blood:
9	chr4:2866369..2868735-chr4:2871007..2873229,2	MCF-7	breast:
10	chr4:2867681..2870567-chr4:2936383..2939288,2	MCF-7	breast:
11	chr4:2872526..2874787-chr4:2876433..2878036,2	K562	blood:
12	chr4:2844708..2848266-chr4:2857886..2861827,4	K562	blood:
13	chr4:2860130..2862463-chr4:2876073..2878049,2	K562	blood:
14	chr4:2873606..2876373-chr4:2925507..2927684,2	MCF-7	breast:
15	chr4:2866956..2870306-chr4:2932983..2937533,4	K562	blood:
16	chr4:2864305..2866761-chr4:2868243..2869773,2	K562	blood:
17	chr4:2871947..2873673-chr4:2935533..2937298,2	MCF-7	breast:
18	chr4:2859689..2861245-chr4:2862909..2865394,2	MCF-7	breast:
19	chr4:2867163..2870465-chr4:2873616..2875440,4	K562	blood:
20	chr4:2859689..2861245-chr4:2862909..2865394,2	MCF-7	breast:
21	chr4:2846265..2848875-chr4:2873594..2875378,2	K562	blood:
22	chr4:2850138..2853377-chr4:2934213..2937642,3	MCF-7	breast:
23	chr4:2868702..2870783-chr4:2881589..2883580,3	K562	blood:
24	chr4:2819892..2821779-chr4:2853270..2855073,2	MCF-7	breast:
25	chr4:2842030..2853279-chr4:2934021..2940851,24	MCF-7	breast:
26	chr4:2848510..2850735-chr4:2868206..2870939,2	K562	blood:
27	chr4:2845095..2847586-chr4:2852811..2854373,2	K562	blood:
28	chr4:2855740..2858209-chr4:2858751..2860482,2	K562	blood:
29	chr4:2876464..2878755-chr4:2882679..2884281,2	K562	blood:
30	chr2:226959307..226961604-chr4:2869808..2871481,2	MCF-7	breast:
31	chr4:2873287..2875371-chr4:2875676..2877933,2	K562	blood:
32	chr4:2876022..2879054-chr4:2934409..2936795,3	MCF-7	breast:
33	chr4:2858420..2863571-chr4:2865919..2871146,8	K562	blood:
34	chr4:2855341..2858315-chr4:2935063..2937111,2	MCF-7	breast:
35	chr4:2804665..2806753-chr4:2851605..2853395,2	MCF-7	breast:
36	chr4:2855740..2858209-chr4:2858751..2860482,2	K562	blood:
37	chr4:2866369..2868735-chr4:2871007..2873229,2	MCF-7	breast:
38	chr4:2857762..2859404-chr4:2861452..2863344,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 1167 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12503220	chr4:2850142-2850143	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527482747	chr4:2850150-2850151	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs550417546	chr4:2850205-2850206	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs573901216	chr4:2850230-2850231	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542796479	chr4:2850272-2850273	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs57763208	chr4:2850273-2850274	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528634200	chr4:2850290-2850291	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs545166003	chr4:2850292-2850293	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs184314272	chr4:2850300-2850301	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs530794593	chr4:2850356-2850357	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs397823169	chr4:2850377-2850378	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs551280534	chr4:2850439-2850440	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs567576092	chr4:2850441-2850442	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs530243107	chr4:2850493-2850494	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs546833462	chr4:2850534-2850535	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs370219884	chr4:2850540-2850541	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs558631397	chr4:2850549-2850550	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs59426248	chr4:2850571-2850572	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs140679049	chr4:2850590-2850591	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs571238228	chr4:2850604-2850605	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs190483814	chr4:2850638-2850639	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs182506348	chr4:2850670-2850671	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs541759638	chr4:2850688-2850689	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs573940879	chr4:2850707-2850708	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs563246468	chr4:2850718-2850719	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs141420323	chr4:2850735-2850736	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs376470199	chr4:2850747-2850748	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs73794816	chr4:2850771-2850772	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs184649042	chr4:2850784-2850785	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs375666086	chr4:2850815-2850816	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs575599690	chr4:2850816-2850817	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs575243820	chr4:2850820-2850821	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs544162309	chr4:2850844-2850845	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs560941264	chr4:2850854-2850855	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs530373401	chr4:2850940-2850941	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs150838852	chr4:2850944-2850945	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs117044894	chr4:2850946-2850947	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs59798370	chr4:2850987-2850988	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs189097123	chr4:2851041-2851042	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs555103777	chr4:2851054-2851055	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs551474708	chr4:2851080-2851081	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs571207060	chr4:2851119-2851120	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs537059776	chr4:2851193-2851194	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs550636249	chr4:2851236-2851237	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs373875677	chr4:2851237-2851238	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs16843459	chr4:2851252-2851253	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs376788353	chr4:2851290-2851291	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs553285827	chr4:2851403-2851404	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs573007743	chr4:2851410-2851411	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs538409695	chr4:2851455-2851456	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region 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:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2846400-2851000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:2846600-2854400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:2846600-2862400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:2846800-2851000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:2846800-2854200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:2846800-2855400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr4:2846800-2855400	Weak transcription	Placenta	Placenta
8	chr4:2846800-2855600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr4:2846800-2857400	Weak transcription	Aorta	Aorta
10	chr4:2846800-2861800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:2846800-2861800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:2846800-2862000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:2846800-2862600	Weak transcription	Esophagus	oesophagus
14	chr4:2847000-2850600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:2847000-2851000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:2847200-2850200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:2847200-2850400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr4:2847200-2850800	Weak transcription	Fetal Brain Female	brain
19	chr4:2847200-2851200	Weak transcription	HSMM	muscle
20	chr4:2847200-2852000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr4:2847200-2853600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr4:2847200-2862200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr4:2847400-2850200	Weak transcription	Psoas Muscle	Psoas
24	chr4:2847400-2850400	Weak transcription	Fetal Intestine Large	intestine
25	chr4:2847400-2850400	Weak transcription	NHDF-Ad	bronchial
26	chr4:2847400-2851000	Weak transcription	Right Atrium	heart
27	chr4:2847400-2851000	Weak transcription	HSMMtube	muscle
28	chr4:2847400-2852800	Weak transcription	Fetal Thymus	thymus
29	chr4:2847400-2854400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr4:2847400-2854400	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr4:2847400-2859800	Weak transcription	A549	lung
32	chr4:2847400-2863600	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr4:2847800-2850200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:2847800-2850400	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr4:2847800-2850600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr4:2847800-2851000	Weak transcription	Brain Substantia Nigra	brain
37	chr4:2847800-2851200	Weak transcription	Fetal Kidney	kidney
38	chr4:2847800-2852000	Enhancers	K562	blood
39	chr4:2847800-2852600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:2847800-2854200	Enhancers	Primary B cells from peripheral blood	blood
41	chr4:2847800-2854200	Weak transcription	NH-A	brain
42	chr4:2847800-2854200	Weak transcription	Osteobl	bone
43	chr4:2847800-2854600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:2847800-2854800	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:2847800-2855400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr4:2847800-2856200	Weak transcription	HMEC	breast
47	chr4:2848000-2850200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr4:2848000-2850200	Weak transcription	Fetal Lung	lung
49	chr4:2848000-2850400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:2848000-2850400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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