Variant report

Variant	esv3453206
Chromosome Location	chr1:247277329-247282727
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	ATF2	chr1:247282209-247282493	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:247282166-247282519	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr1:247282190-247282604	HepG2	liver:	n/a	n/a
4	CBX3	chr1:247280963-247282452	K562	blood:	n/a	n/a
5	CBX3	chr1:247279956-247280480	K562	blood:	n/a	n/a
6	CBX3	chr1:247278814-247282541	K562	blood:	n/a	n/a
7	CBX3	chr1:247279022-247279825	K562	blood:	n/a	n/a
8	CBX3	chr1:247280516-247280801	K562	blood:	n/a	n/a
9	CHD2	chr1:247282281-247282544	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr1:247282300-247282450	HEK293	kidney:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
11	CTCF	chr1:247282300-247282450	NHEK	skin:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
12	CTCF	chr1:247282340-247282490	HVMF	connective:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
13	CTCF	chr1:247282238-247282525	GM12891	blood:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282314-247282327
14	CTCF	chr1:247282184-247282780	SK-N-SH	brain:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282711-247282724 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282664-247282673 chr1:247282314-247282327
15	CTCF	chr1:247282388-247282441	GM20000	blood:	n/a	n/a
16	CTCF	chr1:247282304-247282378	GM13976	blood:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
17	CTCF	chr1:247282320-247282470	HepG2	liver:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
18	CTCF	chr1:247282280-247282430	GM12869	blood:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
19	CTCF	chr1:247282320-247282470	GM12867	blood:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
20	CTCF	chr1:247282225-247282563	H1-hESC	embryonic stem cell:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282314-247282327
21	CTCF	chr1:247282300-247282450	RPTEC	kidney:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
22	CTCF	chr1:247282360-247282510	HCT-116	colon:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
23	CTCF	chr1:247282320-247282470	GM06990	blood:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
24	CTCF	chr1:247282280-247282430	GM06990	blood:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
25	CTCF	chr1:247282420-247282570	GM12865	blood:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
26	CTCF	chr1:247282300-247282450	HepG2	liver:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
27	CTCF	chr1:247282565-247282567	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:247282300-247282450	HRPEpiC	eye:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
29	CTCF	chr1:247282260-247282527	GM12878	blood:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282314-247282327
30	CTCF	chr1:247282400-247282550	RPTEC	kidney:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
31	CTCF	chr1:247282154-247282523	K562	blood:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282314-247282327
32	CTCF	chr1:247282340-247282490	GM12872	blood:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
33	CTCF	chr1:247282266-247282358	GM19239	blood:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
34	CTCF	chr1:247282300-247282450	WERI-Rb-1	eye:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
35	CTCF	chr1:247282380-247282530	HAc	cerebellar:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
36	CTCF	chr1:247282190-247282740	A549	lung:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282711-247282724 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282664-247282673 chr1:247282314-247282327
37	CTCF	chr1:247282360-247282510	HRPEpiC	eye:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
38	CTCF	chr1:247282320-247282470	WERI-Rb-1	eye:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
39	CTCF	chr1:247282280-247282430	HCM	heart:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
40	CTCF	chr1:247282300-247282450	HCFaa	heart:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
41	CTCF	chr1:247282280-247282430	AG09309	skin:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
42	CTCF	chr1:247282317-247282406	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:247282279-247282390	HUVEC	blood vessel:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
44	CTCF	chr1:247282300-247282450	HPF	lung:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
45	CTCF	chr1:247282300-247282450	GM12872	blood:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
46	CTCF	chr1:247282260-247282410	NHDF-neo	bronchial:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
47	CTCF	chr1:247282300-247282450	HCPEpiC	choroid plexus:	n/a	chr1:247282312-247282330 chr1:247282308-247282317 chr1:247282314-247282327
48	CTCF	chr1:247282340-247282490	GM12866	blood:	n/a	chr1:247282440-247282461 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456
49	CTCF	chr1:247282228-247282511	HepG2	liver:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282314-247282327
50	CTCF	chr1:247282249-247282507	ECC-1	luminal epithelium:	n/a	chr1:247282440-247282461 chr1:247282312-247282330 chr1:247282439-247282455 chr1:247282441-247282454 chr1:247282438-247282456 chr1:247282308-247282317 chr1:247282314-247282327

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:247279205-247279255	Jurkat	blood:	n/a
2	chr1:247282458-247282508	NH-A	brain:	n/a
3	chr1:247278828-247278878	HRCEpiC	kidney:	n/a
4	chr1:247282458-247282508	ProgFib	skin:	n/a
5	chr1:247282458-247282508	IMR90	lung:	fetal
6	chr1:247278828-247278878	Jurkat	blood:	n/a
7	chr1:247278828-247278878	PFSK-1	brain:	n/a
8	chr1:247278828-247278878	HMEC	breast:	n/a
9	chr1:247279205-247279255	IMR90	lung:	fetal
10	chr1:247282458-247282508	H1-hESC	embryonic stem cell:	embryo
11	chr1:247278828-247278878	Caco-2	colon:	n/a
12	chr1:247282458-247282508	A549	lung:	n/a
13	chr1:247282458-247282508	GM19239	blood:	n/a
14	chr1:247282458-247282508	MCF-7	breast:	n/a
15	chr1:247279205-247279255	HCF	heart:	n/a
16	chr1:247278828-247278878	U87	brain:	n/a
17	chr1:247282458-247282508	HUVEC	blood vessel:	n/a
18	chr1:247278828-247278878	MCF10A-Er-Src	breast:	n/a
19	chr1:247282458-247282508	GM12878	blood:	n/a
20	chr1:247278828-247278878	HNPCEpiC	eye:	n/a
21	chr1:247278828-247278878	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:247279205-247279255	PrEC	prostate:	n/a
23	chr1:247282458-247282508	GM12892	blood:	n/a
24	chr1:247282458-247282508	HRPEpiC	eye:	n/a
25	chr1:247278828-247278878	HRPEpiC	eye:	n/a
26	chr1:247282458-247282508	BJ	skin:	n/a
27	chr1:247278828-247278878	HAEpiC	amniotic membrane:	n/a
28	chr1:247279205-247279255	NH-A	brain:	n/a
29	chr1:247282458-247282508	PANC-1	pancreas:	n/a
30	chr1:247278828-247278878	HIPEpiC	eye:	n/a
31	chr1:247282458-247282508	HepG2	liver:	n/a
32	chr1:247279205-247279255	Hepatocyte	liver:	n/a
33	chr1:247278828-247278878	HCT-116	colon:	n/a
34	chr1:247279205-247279255	AG09309	skin:	n/a
35	chr1:247278828-247278878	GM19239	blood:	n/a
36	chr1:247278828-247278878	HEEpiC	esophagus:	n/a
37	chr1:247282458-247282508	Hepatocyte	liver:	n/a
38	chr1:247282458-247282508	BE2_C	brain:	n/a
39	chr1:247282458-247282508	Jurkat	blood:	n/a
40	chr1:247279205-247279255	SK-N-SH_RA	brain:	n/a
41	chr1:247278828-247278878	MCF-7	breast:	n/a
42	chr1:247278828-247278878	HRE	kidney:	n/a
43	chr1:247279205-247279255	HIPEpiC	eye:	n/a
44	chr1:247279205-247279255	BJ	skin:	n/a
45	chr1:247282458-247282508	HMEC	breast:	n/a
46	chr1:247279205-247279255	PANC-1	pancreas:	n/a
47	chr1:247278828-247278878	HCPEpiC	choroid plexus:	n/a
48	chr1:247279205-247279255	U87	brain:	n/a
49	chr1:247279205-247279255	BE2_C	brain:	n/a
50	chr1:247278828-247278878	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:247092146..247096759-chr1:247274350..247278356,6	MCF-7	breast:
2	chr1:247262370..247270931-chr1:247272613..247278774,19	MCF-7	breast:
3	chr1:247276067..247278651-chr1:247493890..247496062,2	MCF-7	breast:
4	chr1:247241666..247243646-chr1:247278123..247279948,2	K562	blood:
5	chr1:247273239..247275061-chr1:247277041..247280302,3	K562	blood:
6	chr1:247274786..247276587-chr1:247277453..247279795,2	MCF-7	breast:
7	chr1:247261271..247263933-chr1:247276366..247278097,2	K562	blood:

Variant related genes	Relation type
FGFR3P6	TF binding region
C1orf229	TF binding region
FGFR3P6	CpG island
C1orf229	CpG island
ENSG00000162714	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000135747	chromatin interactions
ENSG00000221953	chromatin interactions
ENSG00000188295	chromatin interactions

Extended variants
information (count: 178 )
Associated
traits (count: 30 )

Variant overlapped rSNPs/rCNVs (count:178 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75493280	chr1:247277350-247277351	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs76331348	chr1:247277355-247277356	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs564647716	chr1:247277412-247277413	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs375704724	chr1:247277416-247277417	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs144689617	chr1:247277440-247277441	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs550322186	chr1:247277448-247277449	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs567239574	chr1:247277454-247277455	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs563656507	chr1:247277460-247277461	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs78176460	chr1:247277540-247277541	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs373405393	chr1:247277543-247277544	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs533165510	chr1:247277572-247277573	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs549697202	chr1:247277584-247277585	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs370724314	chr1:247277621-247277622	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs369515479	chr1:247277724-247277725	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs79991382	chr1:247277728-247277729	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs535244680	chr1:247277770-247277771	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs558339417	chr1:247277815-247277816	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs571670254	chr1:247277816-247277817	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs141497979	chr1:247277817-247277818	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs78281580	chr1:247277832-247277833	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs114743654	chr1:247277833-247277834	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs143842941	chr1:247277835-247277836	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs552838411	chr1:247277880-247277881	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs372802714	chr1:247277902-247277903	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs572760914	chr1:247277937-247277938	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs151113387	chr1:247277940-247277941	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs565058399	chr1:247277959-247277960	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs530555257	chr1:247277975-247277976	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs12068730	chr1:247278012-247278013	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs534126114	chr1:247278018-247278019	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs529685993	chr1:247278082-247278083	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs141060877	chr1:247278088-247278089	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs187239177	chr1:247278118-247278119	Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs60176339	chr1:247278125-247278126	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs534588348	chr1:247278135-247278136	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs553310215	chr1:247278188-247278189	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs571606134	chr1:247278220-247278221	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs112474547	chr1:247278228-247278229	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs537176199	chr1:247278245-247278246	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs556241409	chr1:247278271-247278272	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs557022226	chr1:247278286-247278287	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs567592231	chr1:247278291-247278292	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs536256486	chr1:247278310-247278311	Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs552902348	chr1:247278416-247278417	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs74931093	chr1:247278445-247278446	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs78664116	chr1:247278451-247278452	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs555731259	chr1:247278459-247278460	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs558500048	chr1:247278490-247278491	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs575393669	chr1:247278492-247278493	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs544019042	chr1:247278498-247278499	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:30)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20435627	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247275600-247279200	Flanking Active TSS	HepG2	liver
2	chr1:247276000-247278400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:247276600-247284600	Weak transcription	Right Ventricle	heart
4	chr1:247276800-247278800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:247276800-247278800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:247276800-247283000	Weak transcription	Spleen	Spleen
7	chr1:247277000-247278600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:247278400-247278600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:247278600-247278800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:247278600-247278800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:247278800-247279000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:247278800-247279000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:247278800-247279200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:247279000-247279200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:247279000-247290800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:247279200-247282400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:247282200-247282600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:247282200-247283600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:247282400-247283800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:247282600-247291000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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