Variant report

Variant	esv3388242
Chromosome Location	chr15:40210910-40214408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:40213584-40213598	K562	blood:	n/a	n/a
2	ATF2	chr15:40212646-40213505	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr15:40213055-40213300	HepG2	liver:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
4	ATF3	chr15:40212987-40213349	K562	blood:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
5	ATF3	chr15:40213019-40213368	H1-hESC	embryonic stem cell:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
6	BACH1	chr15:40212357-40213516	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr15:40212964-40213444	K562	blood:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
8	BHLHE40	chr15:40212974-40213463	GM12878	blood:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
9	BHLHE40	chr15:40213016-40213416	HepG2	liver:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
10	BRCA1	chr15:40212171-40212172	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:40213002-40213005	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr15:40213156-40213541	K562	blood:	n/a	n/a
13	CBX3	chr15:40212487-40212892	K562	blood:	n/a	n/a
14	CBX3	chr15:40212976-40213501	K562	blood:	n/a	n/a
15	CCNT2	chr15:40212951-40213473	K562	blood:	n/a	chr15:40213193-40213202
16	CEBPB	chr15:40210749-40211247	IMR90	lung:	n/a	n/a
17	CEBPB	chr15:40213771-40214084	K562	blood:	n/a	n/a
18	CEBPB	chr15:40213784-40214084	IMR90	lung:	n/a	n/a
19	CHD1	chr15:40210279-40213585	H1-hESC	embryonic stem cell:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
20	CHD1	chr15:40212898-40213494	GM12878	blood:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
21	CHD2	chr15:40212747-40212761	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr15:40212494-40212654	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr15:40213252-40213412	K562	blood:	n/a	n/a
24	CHD2	chr15:40212980-40213446	Hela-S3	cervix:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
25	CHD2	chr15:40213069-40213400	GM12878	blood:	n/a	chr15:40213198-40213208
26	CHD2	chr15:40212902-40213124	H1-hESC	embryonic stem cell:	n/a	chr15:40212983-40212990
27	CREB1	chr15:40212888-40213352	A549	lung:	n/a	chr15:40213173-40213186
28	CTBP2	chr15:40211745-40213391	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr15:40212740-40212890	GM12864	blood:	n/a	n/a
30	CTCF	chr15:40212460-40212610	HA-sp	spinal cord:	n/a	chr15:40212461-40212474 chr15:40212460-40212481
31	CTCF	chr15:40213085-40213322	Spleen_OC	spleen:	n/a	chr15:40213145-40213158
32	CTCF	chr15:40213000-40213150	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr15:40212980-40213130	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr15:40212500-40212650	AG10803	skin:	n/a	n/a
35	CTCF	chr15:40213000-40213150	GM12865	blood:	n/a	n/a
36	CTCF	chr15:40213100-40213250	GM06990	blood:	n/a	chr15:40213145-40213158
37	CTCF	chr15:40213102-40213315	GM12892	blood:	n/a	chr15:40213145-40213158
38	CTCF	chr15:40213080-40213230	GM12866	blood:	n/a	chr15:40213145-40213158
39	CTCF	chr15:40212500-40212650	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr15:40213066-40213180	Hela-S3	cervix:	n/a	chr15:40213145-40213158
41	CTCF	chr15:40212867-40213324	K562	blood:	n/a	chr15:40213145-40213158
42	CTCF	chr15:40212982-40213059	GM20000	blood:	n/a	n/a
43	CTCF	chr15:40213046-40213126	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr15:40212640-40212790	HFF	foreskin:	n/a	n/a
45	CTCF	chr15:40212580-40212730	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr15:40213080-40213230	NHLF	lung:	n/a	chr15:40213145-40213158
47	CTCF	chr15:40212456-40212821	ProgFib	skin:	n/a	chr15:40212458-40212476 chr15:40212461-40212474 chr15:40212460-40212481
48	CTCF	chr15:40212560-40212710	GM12872	blood:	n/a	n/a
49	CTCF	chr15:40212980-40213130	GM12865	blood:	n/a	n/a
50	CTCF	chr15:40212960-40213110	GM12874	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:40212502-40212552	AG10803	skin:	n/a
2	chr15:40213280-40213330	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:40213270-40213320	SAEC	small airway:	n/a
4	chr15:40212502-40212552	AG10803	skin:	n/a
5	chr15:40213280-40213330	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:40213270-40213320	SAEC	small airway:	n/a
7	chr15:40213280-40213330	ECC-1	luminal epithelium:	n/a
8	chr15:40213409-40213459	ECC-1	luminal epithelium:	n/a
9	chr15:40213339-40213389	NHBE	bronchial:	n/a
10	chr15:40212176-40212226	RPTEC	kidney:	n/a
11	chr15:40212781-40212831	NHDF-neo	bronchial:	n/a
12	chr15:40212781-40212831	HL-60	blood:	n/a
13	chr15:40212106-40212156	HMEC	breast:	n/a
14	chr15:40213409-40213459	AG10803	skin:	n/a
15	chr15:40213409-40213459	ovcar-3	ovarian:	n/a
16	chr15:40212781-40212831	H1-hESC	embryonic stem cell:	embryo
17	chr15:40213326-40213376	Jurkat	blood:	n/a
18	chr15:40211272-40211322	GM12878	blood:	n/a
19	chr15:40213339-40213389	HRPEpiC	eye:	n/a
20	chr15:40214068-40214118	HEK293	kidney:	embryo
21	chr15:40213270-40213320	K562	blood:	n/a
22	chr15:40214068-40214118	NT2-D1	testis:	n/a
23	chr15:40211272-40211322	HCPEpiC	choroid plexus:	n/a
24	chr15:40213339-40213389	SK-N-SH_RA	brain:	n/a
25	chr15:40212781-40212831	ProgFib	skin:	n/a
26	chr15:40212188-40212238	A549	lung:	n/a
27	chr15:40214068-40214118	PFSK-1	brain:	n/a
28	chr15:40213339-40213389	U87	brain:	n/a
29	chr15:40214068-40214118	HCPEpiC	choroid plexus:	n/a
30	chr15:40213314-40213364	Jurkat	blood:	n/a
31	chr15:40213280-40213330	T-47D	breast:	n/a
32	chr15:40212781-40212831	GM19239	blood:	n/a
33	chr15:40211272-40211322	U87	brain:	n/a
34	chr15:40213280-40213330	Caco-2	colon:	n/a
35	chr15:40211272-40211322	HRCEpiC	kidney:	n/a
36	chr15:40213326-40213376	Hela-S3	cervix:	n/a
37	chr15:40213270-40213320	U87	brain:	n/a
38	chr15:40213270-40213320	HRPEpiC	eye:	n/a
39	chr15:40212106-40212156	H1-hESC	embryonic stem cell:	embryo
40	chr15:40213339-40213389	Caco-2	colon:	n/a
41	chr15:40212781-40212831	Caco-2	colon:	n/a
42	chr15:40212106-40212156	BJ	skin:	n/a
43	chr15:40213280-40213330	SK-N-SH_RA	brain:	n/a
44	chr15:40212781-40212831	HCPEpiC	choroid plexus:	n/a
45	chr15:40214068-40214118	NHDF-neo	bronchial:	n/a
46	chr15:40212188-40212238	HepG2	liver:	n/a
47	chr15:40213270-40213320	HepG2	liver:	n/a
48	chr15:40213314-40213364	T-47D	breast:	n/a
49	chr15:40214068-40214118	AG04449	skin:	fetal
50	chr15:40213314-40213364	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:40211846..40214390-chr15:40224576..40226655,2	K562	blood:
2	chr15:40213124..40213699-chr17:67323085..67323765,2	Hela-S3	cervix:
3	chr15:40209081..40211622-chr15:40223398..40225588,2	K562	blood:
4	chr1:204042666..204043286-chr15:40213090..40213711,2	Hela-S3	cervix:
5	chr15:40211366..40214080-chr15:40223428..40228644,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2AK4-1	chr15:40213228-40213887	XLOC_011218
2	lnc-EIF2AK4-1	chr15:40213228-40213743	XLOC_011218
3	lnc-EIF2AK4-1	chr15:40213271-40218081	ENSG00000246863.2
4	lnc-EIF2AK4-1	chr15:40213243-40213859	ENSG00000246863
5	lnc-EIF2AK4-1	chr15:40213243-40213859	ENSG00000246863.2
6	lnc-EIF2AK4-1	chr15:40213228-40213748	XLOC_011218

Variant related genes	Relation type
ENSG00000246863	TF binding region
GPR176	TF binding region
ENSG00000246863	CpG island
GPR176	CpG island
ENSG00000143842	chromatin interactions
ENSG00000154265	chromatin interactions
ENSG00000128829	chromatin interactions
MYBL1	miRNA target sites
ERBB4	miRNA target sites

Extended variants
information (count: 138 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:138 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143598809	chr15:40210916-40210917	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs538533552	chr15:40210930-40210931	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77433270	chr15:40210992-40210993	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs76167756	chr15:40211027-40211028	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566039099	chr15:40211044-40211045	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs147484444	chr15:40211130-40211131	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs547401811	chr15:40211161-40211162	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs148527115	chr15:40211175-40211176	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556549616	chr15:40211273-40211274	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs74011703	chr15:40211361-40211362	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555974327	chr15:40211391-40211392	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs139095859	chr15:40211405-40211406	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370078610	chr15:40211406-40211407	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200718925	chr15:40211420-40211421	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569726888	chr15:40211477-40211478	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535648971	chr15:40211487-40211488	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs113103637	chr15:40211495-40211496	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs117303939	chr15:40211500-40211501	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs572385562	chr15:40211510-40211511	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540945987	chr15:40211554-40211555	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs558165825	chr15:40211559-40211560	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12911566	chr15:40211633-40211634	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs188691716	chr15:40211635-40211636	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs151083685	chr15:40211682-40211683	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560644205	chr15:40211779-40211780	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529305422	chr15:40211781-40211782	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs572615492	chr15:40211820-40211821	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs34458776	chr15:40211862-40211863	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542825541	chr15:40211901-40211902	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs56107310	chr15:40211934-40211935	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs528818094	chr15:40211963-40211964	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375099528	chr15:40211967-40211968	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12912357	chr15:40211985-40211986	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551779445	chr15:40211989-40211990	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12912359	chr15:40211990-40211991	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370363084	chr15:40212008-40212009	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs570476659	chr15:40212017-40212018	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs532793751	chr15:40212021-40212022	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77245879	chr15:40212031-40212032	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs80137374	chr15:40212050-40212051	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535515092	chr15:40212062-40212063	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs555628598	chr15:40212071-40212072	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs377215097	chr15:40212075-40212076	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143700851	chr15:40212084-40212085	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs148093550	chr15:40212098-40212099	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34575072	chr15:40212104-40212105	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368646413	chr15:40212137-40212138	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs182145795	chr15:40212160-40212161	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs141122559	chr15:40212174-40212175	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs556899221	chr15:40212177-40212178	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Ovarian cancer	21720365	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40194600-40211000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:40199800-40211800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr15:40201400-40211600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:40209000-40212400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr15:40209200-40213400	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr15:40209200-40213800	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr15:40209800-40211000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:40209800-40213800	Active TSS	H1 Cell Line	embryonic stem cell
9	chr15:40210000-40212400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr15:40210000-40213600	Active TSS	H9 Cell Line	embryonic stem cell
11	chr15:40210200-40211000	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr15:40210200-40211000	Enhancers	Hela-S3	cervix
13	chr15:40210200-40211000	Flanking Active TSS	Osteobl	bone
14	chr15:40210200-40211600	Flanking Active TSS	HUVEC	blood vessel
15	chr15:40210200-40212600	Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr15:40210200-40212800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
17	chr15:40210200-40213600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr15:40210200-40213600	Active TSS	NHLF	lung
19	chr15:40210400-40211200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:40210400-40211400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:40210400-40211600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr15:40210400-40212800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
23	chr15:40210400-40213400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr15:40210400-40213400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:40210400-40213600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr15:40210400-40213600	Active TSS	Aorta	Aorta
27	chr15:40210400-40213800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:40210600-40211000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr15:40210600-40211000	Flanking Active TSS	NHEK	skin
30	chr15:40210600-40212600	Active TSS	HMEC	breast
31	chr15:40210600-40212800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr15:40210600-40213000	Active TSS	NH-A	brain
33	chr15:40210600-40213800	Active TSS	HSMM	muscle
34	chr15:40210800-40211000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
35	chr15:40210800-40211000	Bivalent Enhancer	Fetal Brain Male	brain
36	chr15:40210800-40211800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr15:40210800-40212600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
38	chr15:40210800-40212800	Active TSS	Muscle Satellite Cultured Cells	--
39	chr15:40210800-40213400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr15:40210800-40213400	Active TSS	HSMMtube	muscle
41	chr15:40210800-40213600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr15:40210800-40213600	Active TSS	NHDF-Ad	bronchial
43	chr15:40210800-40213800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr15:40211000-40211200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr15:40211000-40211200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:40211000-40211200	Enhancers	Brain Hippocampus Middle	brain
47	chr15:40211000-40211200	Active TSS	NHEK	skin
48	chr15:40211000-40211400	Bivalent/Poised TSS	Fetal Brain Male	brain
49	chr15:40211000-40211400	Bivalent Enhancer	Fetal Lung	lung
50	chr15:40211000-40211600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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