Variant report

Variant	rs1865053
Chromosome Location	chr19:41814412-41814413
allele	A/G
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	POLR2A	chr19:41813835-41814847	A549	lung:	n/a	n/a
2	POLR2A	chr19:41813814-41814889	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr19:41811701-41817543	SK-N-MC	brain:	n/a	n/a
4	CTCF	chr19:41811702-41817527	A549	lung:	n/a	chr19:41814589-41814607 chr19:41814590-41814606 chr19:41814584-41814605 chr19:41814591-41814604 chr19:41814591-41814604 chr19:41813852-41813873 chr19:41813850-41813868 chr19:41814601-41814614
5	CTCF	chr19:41814289-41814801	A549	lung:	n/a	chr19:41814589-41814607 chr19:41814590-41814606 chr19:41814584-41814605 chr19:41814591-41814604 chr19:41814591-41814604 chr19:41814601-41814614
6	MBD4	chr19:41814198-41814924	HepG2	liver:	n/a	n/a
7	SMC3	chr19:41813494-41815570	SK-N-SH	brain:	n/a	chr19:41814591-41814605
8	RAD21	chr19:41814227-41814914	HCT-116	colon:	n/a	chr19:41814587-41814606 chr19:41814589-41814601 chr19:41814600-41814613 chr19:41814597-41814616 chr19:41814591-41814605
9	EP300	chr19:41814349-41814757	GM12878	blood:	n/a	n/a
10	WRNIP1	chr19:41814273-41815305	GM12878	blood:	n/a	n/a
11	POLR2A	chr19:41813221-41816825	GM12878	blood:	n/a	n/a
12	POLR2A	chr19:41813405-41816912	HepG2	liver:	n/a	n/a
13	ZNF143	chr19:41814118-41814800	K562	blood:	n/a	n/a
14	POLR2A	chr19:41813668-41816626	GM18505	blood:	n/a	n/a
15	POU2F2	chr19:41814403-41814717	GM12878	blood:	n/a	chr19:41814686-41814695 chr19:41814683-41814697 chr19:41814687-41814694
16	POLR2A	chr19:41814046-41816774	PBDE	blood:	n/a	n/a
17	TEAD4	chr19:41814370-41814822	K562	blood:	n/a	n/a
18	TEAD4	chr19:41814134-41814940	K562	blood:	n/a	n/a
19	TBL1XR1	chr19:41814351-41814818	K562	blood:	n/a	n/a
20	POLR2A	chr19:41813712-41816830	GM12891	blood:	n/a	n/a
21	FOXM1	chr19:41814202-41814841	GM12878	blood:	n/a	n/a
22	RAD21	chr19:41814385-41814774	HepG2	liver:	n/a	chr19:41814587-41814606 chr19:41814589-41814601 chr19:41814600-41814613 chr19:41814597-41814616 chr19:41814591-41814605
23	POLR2A	chr19:41813813-41815574	GM12891	blood:	n/a	n/a
24	NFIC	chr19:41814178-41814887	HepG2	liver:	n/a	n/a
25	RAD21	chr19:41814370-41814760	HepG2	liver:	n/a	chr19:41814587-41814606 chr19:41814589-41814601 chr19:41814600-41814613 chr19:41814597-41814616 chr19:41814591-41814605
26	POLR2A	chr19:41814216-41814863	Hela-S3	cervix:	n/a	n/a
27	RELA	chr19:41814218-41815031	GM12878	blood:	n/a	chr19:41814551-41814560 chr19:41814551-41814560
28	STAT5A	chr19:41813753-41816690	GM12878	blood:	n/a	chr19:41814315-41814323 chr19:41813977-41813985 chr19:41816016-41816024
29	POLR2A	chr19:41809524-41818013	K562	blood:	n/a	n/a
30	POLR2A	chr19:41813354-41817333	K562	blood:	n/a	n/a
31	FOXM1	chr19:41814140-41814943	GM12878	blood:	n/a	n/a
32	POLR2A	chr19:41814139-41814898	H1-hESC	embryonic stem cell:	n/a	n/a
33	ZMIZ1	chr19:41814393-41814955	K562	blood:	n/a	n/a
34	CREB1	chr19:41814285-41814835	A549	lung:	n/a	n/a
35	RCOR1	chr19:41814165-41815010	GM12878	blood:	n/a	n/a
36	ZBTB33	chr19:41814380-41815435	A549	lung:	n/a	n/a
37	BRCA1	chr19:41814377-41814733	GM12878	blood:	n/a	n/a
38	SIX5	chr19:41814064-41817340	A549	lung:	n/a	n/a
39	USF1	chr19:41814309-41816830	A549	lung:	n/a	n/a
40	RAD21	chr19:41814366-41814884	IMR90	lung:	n/a	chr19:41814587-41814606 chr19:41814589-41814601 chr19:41814600-41814613 chr19:41814597-41814616 chr19:41814591-41814605
41	SIN3AK20	chr19:41814155-41816958	A549	lung:	n/a	n/a
42	POLR2A	chr19:41814184-41814867	HepG2	liver:	n/a	n/a
43	CTCF	chr19:41814317-41814911	K562	blood:	n/a	chr19:41814589-41814607 chr19:41814590-41814606 chr19:41814584-41814605 chr19:41814591-41814604 chr19:41814591-41814604 chr19:41814601-41814614
44	BCL3	chr19:41813942-41815083	K562	blood:	n/a	chr19:41814588-41814596
45	ELF1	chr19:41814232-41814923	GM12878	blood:	n/a	n/a
46	POLR2A	chr19:41814411-41814978	ProgFib	skin:	n/a	n/a
47	ARID3A	chr19:41814405-41814774	HepG2	liver:	n/a	n/a
48	CTCF	chr19:41814151-41814956	GM12878	blood:	n/a	chr19:41814589-41814607 chr19:41814590-41814606 chr19:41814584-41814605 chr19:41814591-41814604 chr19:41814591-41814604 chr19:41814601-41814614
49	POLR2A	chr19:41812504-41817492	U87	brain:	n/a	n/a
50	RAD21	chr19:41814293-41814766	H1-hESC	embryonic stem cell:	n/a	chr19:41814587-41814606 chr19:41814589-41814601 chr19:41814600-41814613 chr19:41814597-41814616 chr19:41814591-41814605

No.	Distal block	Cell Line	Cell type
1	chr19:41799355..41806261-chr19:41812914..41817863,9	MCF-7	breast:
2	chr19:41808201..41810426-chr19:41812838..41816052,5	K562	blood:
3	chr19:41766963..41771332-chr19:41813075..41817628,7	K562	blood:
4	chr19:41711943..41714623-chr19:41813301..41815470,3	MCF-7	breast:
5	chr19:41814082..41814803-chr19:41860791..41861367,2	K562	blood:
6	chr19:41813131..41816938-chr19:41856231..41860417,4	MCF-7	breast:
7	chr19:41813982..41818537-chr19:41824784..41829010,7	MCF-7	breast:
8	chr19:41709937..41710810-chr19:41814166..41815131,2	MCF-7	breast:
9	chr19:41767589..41772847-chr19:41812402..41817981,15	MCF-7	breast:
10	chr19:41766631..41773289-chr19:41812153..41817614,9	K562	blood:

Variant related genes	Relation type
CCDC97	TF binding region
ENSG00000255730	Chromatin interaction
ENSG00000142039	Chromatin interaction
ENSG00000105329	Chromatin interaction
ENSG00000105323	Chromatin interaction
ENSG00000142046	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10410836	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10421990	0.94[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1056854	0.91[CEU][hapmap];0.82[TSI][hapmap];0.89[EUR][1000 genomes]
rs11466359	0.92[EUR][1000 genomes]
rs11879562	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11880564	0.92[EUR][1000 genomes]
rs11881940	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs11881953	0.88[EUR][1000 genomes]
rs11882467	0.95[CHB][hapmap]
rs12327659	0.91[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12462203	0.90[CHB][hapmap]
rs12972266	0.98[EUR][1000 genomes]
rs12974323	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12974420	0.91[CEU][hapmap];0.89[TSI][hapmap];0.92[EUR][1000 genomes]
rs12975585	0.95[CHB][hapmap];0.80[CHD][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs12975920	0.98[ASN][1000 genomes]
rs12976536	0.92[EUR][1000 genomes]
rs12978323	0.85[CHB][hapmap];0.80[CHD][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs12980298	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12980480	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.93[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12980839	0.94[ASN][1000 genomes]
rs12980942	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs12981053	0.81[EUR][1000 genomes]
rs12983047	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12984160	1.00[CEU][hapmap];0.96[TSI][hapmap];0.98[EUR][1000 genomes]
rs12985162	0.91[CEU][hapmap];0.85[TSI][hapmap];0.89[EUR][1000 genomes]
rs12985339	0.91[CEU][hapmap];0.89[TSI][hapmap];0.92[EUR][1000 genomes]
rs13345456	1.00[ASN][1000 genomes]
rs16958994	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16958996	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16958999	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1865051	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1865052	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2053086	0.91[CEU][hapmap];0.89[TSI][hapmap];0.92[EUR][1000 genomes]
rs2241718	1.00[CEU][hapmap];0.93[TSI][hapmap];0.91[EUR][1000 genomes]
rs2241719	0.92[EUR][1000 genomes]
rs2241720	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs2304230	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2304234	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs34075897	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34322801	0.94[EUR][1000 genomes]
rs34945449	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35501756	0.95[EUR][1000 genomes]
rs35812313	0.92[EUR][1000 genomes]
rs3745295	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3752705	0.91[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.92[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3786555	0.81[ASN][1000 genomes]
rs3816052	0.94[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3826714	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4456618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4802111	0.90[CHB][hapmap]
rs4802112	0.95[CHB][hapmap];0.88[JPT][hapmap]
rs4802113	0.89[CHB][hapmap]
rs4803448	0.90[CHB][hapmap]
rs4803449	0.90[CHB][hapmap]
rs6508974	0.90[CHB][hapmap]
rs66724427	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67511749	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67744888	0.92[EUR][1000 genomes]
rs6957	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7245398	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7246525	0.90[CHB][hapmap]
rs7248164	0.94[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7254679	0.82[CEU][hapmap];0.94[ASN][1000 genomes]
rs7256416	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7256856	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7257310	1.00[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.96[TSI][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7257742	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7257825	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7258749	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8103839	0.91[CEU][hapmap];0.89[TSI][hapmap];0.92[EUR][1000 genomes]
rs8105161	1.00[CEU][hapmap];0.86[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8105901	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs8109167	0.82[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8109627	0.95[CHB][hapmap];0.94[CHD][hapmap];0.88[JPT][hapmap];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv17637	chr19:41770228-41815282	Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv911769	chr19:41813676-41845801	Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs1865053	BAX	cis	cerebellum	SCAN
rs1865053	FLT3LG	cis	cerebellum	SCAN
rs1865053	TSKS	cis	parietal	SCAN
rs1865053	PLEKHA4	cis	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41780200-41815800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr19:41788600-41815400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr19:41801600-41814600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr19:41806200-41814600	Strong transcription	HSMM	muscle
5	chr19:41811200-41814600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr19:41812200-41814600	Genic enhancers	Rectal Mucosa Donor 29	rectum
7	chr19:41812400-41815800	Flanking Active TSS	Primary T cells from cord blood	blood
8	chr19:41812400-41815800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
9	chr19:41812600-41815000	Genic enhancers	A549	lung
10	chr19:41812600-41815200	Weak transcription	Ovary	ovary
11	chr19:41812600-41815600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr19:41812600-41815600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
13	chr19:41812600-41815800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
14	chr19:41812600-41815800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr19:41812800-41815000	Weak transcription	Aorta	Aorta
16	chr19:41812800-41815400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr19:41812800-41815400	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr19:41812800-41815600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr19:41812800-41816000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr19:41813000-41815200	Enhancers	HUVEC	blood vessel
21	chr19:41813000-41815800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
22	chr19:41813000-41815800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr19:41813000-41816000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr19:41813200-41814600	Weak transcription	NHLF	lung
25	chr19:41813200-41815400	Enhancers	Small Intestine	intestine
26	chr19:41813200-41815600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
27	chr19:41813200-41815600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
28	chr19:41813200-41816000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr19:41813200-41816000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr19:41813400-41815200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr19:41813400-41816000	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr19:41813600-41814800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr19:41813800-41814600	Enhancers	Primary hematopoietic stem cells	blood
34	chr19:41813800-41814600	Genic enhancers	Fetal Muscle Trunk	muscle
35	chr19:41813800-41814600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr19:41813800-41815000	Enhancers	Pancreas	Pancrea
37	chr19:41813800-41815200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr19:41813800-41815200	Enhancers	Stomach Mucosa	stomach
39	chr19:41813800-41815200	Transcr. at gene 5' and 3'	Dnd41	blood
40	chr19:41814000-41814600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr19:41814000-41814600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr19:41814000-41814600	Enhancers	Brain Cingulate Gyrus	brain
43	chr19:41814000-41814600	Enhancers	Brain Hippocampus Middle	brain
44	chr19:41814000-41814600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr19:41814000-41814600	Enhancers	Brain Substantia Nigra	brain
46	chr19:41814000-41814600	Enhancers	Fetal Heart	heart
47	chr19:41814000-41814600	Genic enhancers	Placenta	Placenta
48	chr19:41814000-41814800	Genic enhancers	HUES6 Cell Line	embryonic stem cell
49	chr19:41814000-41815000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr19:41814000-41815000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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