Variant report

Variant	rs1414367
Chromosome Location	chr1:93647106-93647107
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF384	chr1:93645246-93647334	K562	blood:	n/a	n/a
2	POLR2A	chr1:93646626-93647109	SK-N-SH	brain:	n/a	n/a
3	POLR2A	chr1:93645008-93647230	SK-N-MC	brain:	n/a	n/a
4	PML	chr1:93644916-93647169	K562	blood:	n/a	n/a
5	MAX	chr1:93644987-93647107	GM12878	blood:	n/a	n/a
6	CBX3	chr1:93645030-93647181	K562	blood:	n/a	n/a
7	POLR2A	chr1:93645046-93647124	GM12878	blood:	n/a	n/a
8	PML	chr1:93645059-93647177	K562	blood:	n/a	n/a
9	POLR2A	chr1:93645226-93647161	K562	blood:	n/a	n/a
10	POU2F2	chr1:93646722-93647149	GM12878	blood:	n/a	chr1:93646754-93646766 chr1:93646760-93646772
11	GATA1	chr1:93644434-93647154	PBDE	blood:	n/a	n/a
12	SRF	chr1:93646955-93647119	GM12878	blood:	n/a	chr1:93647044-93647062 chr1:93647044-93647058 chr1:93647042-93647059
13	TBL1XR1	chr1:93645025-93647145	K562	blood:	n/a	n/a
14	NFIC	chr1:93644930-93647114	GM12878	blood:	n/a	chr1:93645104-93645121
15	POLR2A	chr1:93644987-93647172	GM12878	blood:	n/a	n/a
16	PML	chr1:93644875-93647216	GM12878	blood:	n/a	n/a
17	POLR2A	chr1:93645076-93647191	GM12892	blood:	n/a	n/a
18	POLR2A	chr1:93644941-93647205	GM12892	blood:	n/a	n/a
19	POLR2A	chr1:93644943-93647243	GM12892	blood:	n/a	n/a
20	POLR2A	chr1:93644780-93647219	GM12878	blood:	n/a	n/a
21	STAT5A	chr1:93645619-93647150	K562	blood:	n/a	chr1:93646756-93646768
22	UBTF	chr1:93645208-93647240	K562	blood:	n/a	n/a
23	POLR2A	chr1:93645087-93647114	GM12891	blood:	n/a	n/a
24	POLR2A	chr1:93646635-93647175	GM12892	blood:	n/a	n/a
25	HCFC1	chr1:93644851-93647227	Hela-S3	cervix:	n/a	n/a
26	NR2F2	chr1:93644853-93647172	K562	blood:	n/a	n/a
27	MAX	chr1:93644965-93647154	HCT-116	colon:	n/a	n/a
28	POLR2A	chr1:93645083-93647150	PBDE	blood:	n/a	n/a
29	MYC	chr1:93644945-93647113	MCF10A-Er-Src	breast:	n/a	n/a
30	FOXM1	chr1:93644930-93647169	GM12878	blood:	n/a	n/a
31	MXI1	chr1:93643106-93647204	SK-N-SH	brain:	n/a	n/a
32	MTA3	chr1:93644947-93647185	GM12878	blood:	n/a	n/a
33	POLR2A	chr1:93645121-93647334	K562	blood:	n/a	n/a
34	POLR2A	chr1:93646673-93647153	GM12891	blood:	n/a	n/a
35	STAT5A	chr1:93644827-93647186	GM12878	blood:	n/a	chr1:93646756-93646768
36	EP300	chr1:93645724-93647198	K562	blood:	n/a	n/a
37	CEBPD	chr1:93646566-93647128	K562	blood:	n/a	n/a
38	FOXM1	chr1:93645832-93647200	GM12878	blood:	n/a	n/a
39	JUND	chr1:93645057-93647122	K562	blood:	n/a	n/a
40	TEAD4	chr1:93644775-93647245	K562	blood:	n/a	n/a
41	POLR2A	chr1:93645014-93647157	GM12891	blood:	n/a	n/a
42	CREB1	chr1:93645005-93647210	GM12878	blood:	n/a	n/a
43	POLR2A	chr1:93645074-93647112	K562	blood:	n/a	n/a
44	MYC	chr1:93645018-93647120	K562	blood:	n/a	n/a
45	POLR2A	chr1:93645038-93647234	HL-60	blood:	n/a	n/a
46	POLR2A	chr1:93645017-93648065	K562	blood:	n/a	n/a
47	ZNF384	chr1:93644783-93647140	GM12878	blood:	n/a	n/a
48	POLR2A	chr1:93644949-93647174	GM12878	blood:	n/a	n/a
49	EP300	chr1:93645003-93647143	GM12878	blood:	n/a	chr1:93645464-93645480 chr1:93645250-93645264
50	POLR2A	chr1:93644972-93647162	HUVEC	blood vessel:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:93646436..93648655-chr1:93649128..93651359,3	MCF-7	breast:
2	chr1:93543004..93547095-chr1:93643826..93649088,10	K562	blood:
3	chr1:93645225..93647960-chr1:93665324..93667847,2	MCF-7	breast:
4	chr1:93645217..93647483-chr1:93810016..93813905,4	K562	blood:
5	chr1:93543004..93547588-chr1:93644888..93649088,6	K562	blood:
6	chr1:93646277..93649734-chr1:93664673..93670683,6	K562	blood:
7	chr1:93644831..93648972-chr1:93800687..93805034,4	K562	blood:
8	chr1:93296314..93299115-chr1:93644282..93648010,4	K562	blood:

No data

Variant related genes	Relation type
TMED5	TF binding region
ENSG00000223745	Chromatin interaction
ENSG00000225297	Chromatin interaction
ENSG00000117505	Chromatin interaction
ENSG00000143033	Chromatin interaction
ENSG00000122406	Chromatin interaction

Extended variants
information (count: 111 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs10782958	0.81[EUR][1000 genomes]
rs1081526	0.87[AMR][1000 genomes]
rs10874765	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs10874767	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap];0.80[EUR][1000 genomes]
rs10874771	0.81[EUR][1000 genomes]
rs11164874	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11164878	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11164882	0.85[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11164888	0.80[EUR][1000 genomes]
rs11164889	0.80[EUR][1000 genomes]
rs11164890	0.80[EUR][1000 genomes]
rs11164911	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap]
rs11582703	0.81[EUR][1000 genomes]
rs11586323	0.86[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12057476	1.00[ASW][hapmap];0.95[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12064785	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12066315	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12067005	0.91[ASW][hapmap];0.92[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12070900	0.84[CEU][hapmap];0.94[YRI][hapmap];0.81[EUR][1000 genomes]
rs12071627	0.81[EUR][1000 genomes]
rs12080715	0.80[EUR][1000 genomes]
rs12085959	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs12087466	0.86[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12088338	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12090723	0.81[EUR][1000 genomes]
rs12094547	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12731675	0.81[EUR][1000 genomes]
rs12731809	0.81[EUR][1000 genomes]
rs1323626	0.87[AMR][1000 genomes]
rs1323628	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes]
rs1535698	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs1535700	1.00[CEU][hapmap]
rs1570528	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap]
rs17131699	1.00[ASW][hapmap];0.83[LWK][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2391227	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2484485	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2749735	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2783492	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2783498	0.92[CEU][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2783506	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2815408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2815409	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2815410	0.93[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2815411	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2815412	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2815413	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs2815414	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs36057148	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4573531	0.81[EUR][1000 genomes]
rs4847239	1.00[CEU][hapmap];0.87[YRI][hapmap]
rs4847409	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap]
rs485622	0.85[EUR][1000 genomes]
rs488646	1.00[CEU][hapmap]
rs504810	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs505531	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs506556	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs519723	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap];0.84[EUR][1000 genomes]
rs522999	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs546	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs556888	1.00[CEU][hapmap]
rs55701931	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs559397	0.81[EUR][1000 genomes]
rs56303209	0.81[EUR][1000 genomes]
rs566743	0.81[EUR][1000 genomes]
rs571212	1.00[CEU][hapmap];0.83[GIH][hapmap];0.92[TSI][hapmap];0.84[EUR][1000 genomes]
rs573056	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap];0.89[EUR][1000 genomes]
rs581825	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs587754	0.81[EUR][1000 genomes]
rs605759	0.86[EUR][1000 genomes]
rs615416	0.92[EUR][1000 genomes]
rs626714	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap];0.80[EUR][1000 genomes]
rs628714	1.00[CEU][hapmap]
rs629153	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs633789	0.93[CEU][hapmap];0.92[TSI][hapmap]
rs637198	0.80[EUR][1000 genomes]
rs6541351	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs658178	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs658877	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs661566	0.83[EUR][1000 genomes]
rs662546	0.83[EUR][1000 genomes]
rs6657587	0.80[EUR][1000 genomes]
rs6664886	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs6667701	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap];0.80[EUR][1000 genomes]
rs667680	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs668944	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap]
rs6701250	1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[MEX][hapmap];0.96[TSI][hapmap]
rs670650	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs671559	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs693872	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs698926	0.87[AMR][1000 genomes]
rs71510760	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7519163	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[TSI][hapmap]
rs7551635	0.81[EUR][1000 genomes]
rs7555292	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs771452	0.87[AMR][1000 genomes]
rs771457	1.00[CEU][hapmap];0.94[YRI][hapmap];0.87[AMR][1000 genomes]
rs771459	1.00[CEU][hapmap]
rs771460	0.87[AMR][1000 genomes]
rs771463	1.00[CEU][hapmap];0.96[TSI][hapmap]
rs771464	0.81[AMR][1000 genomes]
rs771466	0.87[AMR][1000 genomes]
rs771472	0.87[AMR][1000 genomes]
rs771474	0.87[AMR][1000 genomes]
rs771480	0.87[AMR][1000 genomes]
rs797660	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs797669	0.82[EUR][1000 genomes]
rs809515	0.84[EUR][1000 genomes]
rs812789	1.00[CEU][hapmap]
rs9432700	0.81[EUR][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	nsv830614	chr1:93465978-93678700	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv830625	chr1:93566378-93735246	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs1414367	TMED5	cis	cerebellum	SCAN
rs1414367	RP4-717I23.3	cis	Adipose Subcutaneous	GTEx
rs1414367	RP4-717I23.3	cis	Nerve Tibial	GTEx
rs1414367	RP4-717I23.3	cis	Skin Sun Exposed Lower leg	GTEx
rs1414367	RP4-717I23.3	cis	Artery Aorta	GTEx
rs1414367	RP4-717I23.3	cis	lung	GTEx
rs1414367	RP4-717I23.3	cis	Stomach	GTEx
rs1414367	RP4-717I23.3	cis	Muscle Skeletal	GTEx
rs1414367	RP4-717I23.3	cis	Artery Tibial	GTEx
rs1414367	RP4-717I23.3	cis	Esophagus Muscularis	GTEx
rs1414367	TMED5	cis	parietal	SCAN
rs1414367	RP4-717I23.3	cis	Heart Left Ventricle	GTEx
rs1414367	TMED5	Cis_1M	lymphoblastoid	RTeQTL
rs1414367	RP4-717I23.3	cis	Whole Blood	GTEx
rs1414367	RP4-717I23.3	cis	Thyroid	GTEx
rs1414367	RP4-717I23.3	cis	Esophagus Mucosa	GTEx

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93642200-93647200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:93642600-93647800	Active TSS	K562	blood
3	chr1:93642800-93647200	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr1:93643000-93647600	Active TSS	NHLF	lung
5	chr1:93643000-93648400	Active TSS	GM12878-XiMat	blood
6	chr1:93643200-93647400	Active TSS	A549	lung
7	chr1:93643200-93647600	Active TSS	HMEC	breast
8	chr1:93643400-93647200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:93643600-93647200	Active TSS	H1 Cell Line	embryonic stem cell
10	chr1:93643600-93647200	Active TSS	H9 Cell Line	embryonic stem cell
11	chr1:93643600-93647400	Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr1:93643600-93647600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:93643600-93647800	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr1:93643800-93647200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:93643800-93647200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:93643800-93647200	Active TSS	Colonic Mucosa	Colon
17	chr1:93644000-93647800	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr1:93644200-93647200	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr1:93644200-93647200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr1:93644200-93647200	Active TSS	Fetal Intestine Large	intestine
21	chr1:93644200-93647200	Active TSS	Fetal Kidney	kidney
22	chr1:93644200-93647200	Active TSS	HSMMtube	muscle
23	chr1:93644200-93648000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:93644400-93647200	Active TSS	Brain Anterior Caudate	brain
25	chr1:93644400-93647200	Active TSS	Rectal Smooth Muscle	rectum
26	chr1:93644400-93648000	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr1:93644400-93648000	Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr1:93644600-93647200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:93644600-93647200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr1:93644600-93647200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr1:93644600-93647200	Active TSS	Fetal Heart	heart
32	chr1:93644600-93647400	Active TSS	Primary T killer memory cells from peripheral blood	blood
33	chr1:93644600-93647400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:93644600-93647600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:93644800-93647200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr1:93644800-93647200	Active TSS	Fetal Muscle Trunk	muscle
37	chr1:93644800-93647200	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr1:93644800-93647400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr1:93645800-93647200	Active TSS	Primary T cells fromperipheralblood	blood
40	chr1:93646000-93647200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr1:93646000-93647200	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr1:93646400-93647200	Active TSS	Fetal Brain Male	brain
43	chr1:93646400-93647400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:93646600-93647200	Active TSS	Brain Germinal Matrix	brain
45	chr1:93646600-93647200	Enhancers	Colon Smooth Muscle	Colon
46	chr1:93646600-93647200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr1:93646600-93647200	Flanking Active TSS	Fetal Intestine Small	intestine
48	chr1:93646600-93647400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr1:93646600-93647600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:93646600-93660400	Weak transcription	Lung	lung

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