Variant report

Variant	rs10737004
Chromosome Location	chr10:1039019-1039020
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:46)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:46 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr10:1039019-1039293	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr10:1038741-1040230	HepG2	liver:	n/a	n/a
3	POLR2A	chr10:1038845-1039274	GM12892	blood:	n/a	n/a
4	HEY1	chr10:1038726-1039242	K562	blood:	n/a	n/a
5	POLR2A	chr10:1038813-1039104	H1-hESC	embryonic stem cell:	n/a	n/a
6	ZNF384	chr10:1038887-1039144	K562	blood:	n/a	n/a
7	POLR2A	chr10:1038792-1039777	K562	blood:	n/a	n/a
8	POLR2A	chr10:1038739-1039772	GM12891	blood:	n/a	n/a
9	POLR2A	chr10:1038409-1042321	A549	lung:	n/a	n/a
10	POLR2A	chr10:1038892-1039370	K562	blood:	n/a	n/a
11	MAX	chr10:1038984-1039101	GM12878	blood:	n/a	n/a
12	POLR2A	chr10:1038806-1039359	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr10:1038716-1040562	GM12892	blood:	n/a	n/a
14	POLR2A	chr10:1038754-1039275	Hela-S3	cervix:	n/a	n/a
15	POU2F2	chr10:1038395-1039060	GM12878	blood:	n/a	chr10:1038622-1038640 chr10:1038625-1038636 chr10:1038626-1038636
16	POLR2A	chr10:1038716-1039253	GM12891	blood:	n/a	n/a
17	MAZ	chr10:1038967-1039102	GM12878	blood:	n/a	n/a
18	POLR2A	chr10:1038352-1039194	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr10:1038823-1039176	GM12878	blood:	n/a	n/a
20	ZNF384	chr10:1038257-1039148	GM12878	blood:	n/a	n/a
21	POLR2A	chr10:1038478-1039299	K562	blood:	n/a	n/a
22	CEBPB	chr10:1038864-1039169	K562	blood:	n/a	n/a
23	POLR2A	chr10:1038441-1039192	HepG2	liver:	n/a	n/a
24	FOS	chr10:1038925-1039123	MCF10A-Er-Src	breast:	n/a	n/a
25	WRNIP1	chr10:1038858-1039040	GM12878	blood:	n/a	n/a
26	USF2	chr10:1038923-1039119	K562	blood:	n/a	n/a
27	POLR2A	chr10:1038787-1039280	GM12891	blood:	n/a	n/a
28	BHLHE40	chr10:1038483-1039064	GM12878	blood:	n/a	n/a
29	EP300	chr10:1038490-1039033	GM12878	blood:	n/a	n/a
30	POLR2A	chr10:1038686-1039840	GM12892	blood:	n/a	n/a
31	POLR2A	chr10:1038907-1039197	GM12891	blood:	n/a	n/a
32	MXI1	chr10:1039011-1039163	GM12878	blood:	n/a	n/a
33	POLR2A	chr10:1038810-1039392	K562	blood:	n/a	n/a
34	POLR2A	chr10:1038332-1040432	GM12878	blood:	n/a	n/a
35	POLR2A	chr10:1038732-1040375	GM12892	blood:	n/a	n/a
36	USF2	chr10:1038966-1039128	GM12878	blood:	n/a	n/a
37	TBP	chr10:1038419-1039083	GM12878	blood:	n/a	n/a
38	CEBPB	chr10:1038866-1039201	A549	lung:	n/a	n/a
39	CEBPB	chr10:1038878-1039223	HepG2	liver:	n/a	n/a
40	STAT3	chr10:1038510-1039051	GM12878	blood:	n/a	n/a
41	POLR2A	chr10:1038780-1039790	H1-hESC	embryonic stem cell:	n/a	n/a
42	EBF1	chr10:1038360-1039097	GM12878	blood:	n/a	n/a
43	POLR2A	chr10:1038489-1040257	GM12878	blood:	n/a	n/a
44	POLR2A	chr10:1038681-1039860	GM12878	blood:	n/a	n/a
45	POLR2A	chr10:1038770-1039346	K562	blood:	n/a	n/a
46	POLR2A	chr10:1038953-1039147	Hela-S3	cervix:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:1032021..1036235-chr10:1037103..1040442,8	MCF-7	breast:
2	chr10:1033990..1039615-chr10:1093691..1098446,7	MCF-7	breast:
3	chr10:1032460..1036223-chr10:1037053..1039174,5	K562	blood:
4	chr10:1037288..1039582-chr10:1100848..1103600,2	K562	blood:
5	chr10:969783..971974-chr10:1038430..1041356,2	K562	blood:
6	chr10:908096..910610-chr10:1038857..1040651,2	K562	blood:
7	chr10:1038435..1041115-chr10:1083089..1086536,3	K562	blood:
8	chr10:1037105..1042640-chr10:1092491..1096899,6	K562	blood:
9	chr10:1037199..1043943-chr10:1053362..1060206,13	K562	blood:
10	chr10:1024264..1026844-chr10:1037522..1040068,2	MCF-7	breast:
11	chr10:974510..978997-chr10:1037469..1040062,8	K562	blood:
12	chr10:974510..978091-chr10:1036448..1040062,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000205740	TF binding region
ENSG00000047056	Chromatin interaction
ENSG00000205740	Chromatin interaction
ENSG00000229869	Chromatin interaction
ENSG00000107929	Chromatin interaction
ENSG00000067064	Chromatin interaction
ENSG00000107937	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10752022	1.00[CEU][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10795302	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10795303	0.86[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10795306	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10904597	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11250222	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11250232	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11250238	1.00[CHB][hapmap]
rs11253536	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11253548	0.89[ASN][1000 genomes]
rs11253552	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11253565	0.98[ASN][1000 genomes]
rs11253566	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253567	1.00[CEU][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1135416	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11599238	0.89[ASN][1000 genomes]
rs11599483	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11599573	0.89[ASN][1000 genomes]
rs17131848	0.81[ASN][1000 genomes]
rs1904671	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2387213	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2620942	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3207775	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs3763720	0.98[ASN][1000 genomes]
rs3793778	1.00[CHB][hapmap]
rs4880746	0.87[ASN][1000 genomes]
rs4880754	0.81[ASN][1000 genomes]
rs4880758	1.00[CHB][hapmap]
rs4881549	0.89[ASN][1000 genomes]
rs4881550	0.89[ASN][1000 genomes]
rs6560863	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7070724	1.00[CEU][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7076107	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7080072	0.85[CHB][hapmap]
rs7084337	0.86[EUR][1000 genomes]
rs7094331	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7095853	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72478233	0.89[ASN][1000 genomes]
rs7918118	1.00[CEU][hapmap];0.91[YRI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916591	chr10:224406-1088734	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1054659	chr10:611444-1133578	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
4	nsv466697	chr10:734229-1129527	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv549765	chr10:734229-1129527	Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv530116	chr10:776548-1401075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv1052540	chr10:887562-1300134	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv540407	chr10:887562-1300134	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv533861	chr10:945438-1382068	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
10	nsv530117	chr10:945438-1729634	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv540408	chr10:955835-1260680	Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
12	nsv817532	chr10:964660-1885945	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
13	esv2753756	chr10:985264-1052950	Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv1050577	chr10:986723-1277854	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv540409	chr10:986723-1277854	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv949405	chr10:1010464-1376105	Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
17	nsv1048254	chr10:1016006-1146595	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
18	esv1812809	chr10:1021156-1051728	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
19	esv1813158	chr10:1021156-1062915	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
20	esv1831483	chr10:1021156-1062915	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
21	nsv1040178	chr10:1024910-1126104	Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
22	nsv540410	chr10:1024910-1126104	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10737004	GTPBP4///IDI2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1035000-1094000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:1035400-1040000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr10:1035400-1040400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr10:1035600-1043600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr10:1035800-1046800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr10:1035800-1066200	Strong transcription	NH-A	brain
7	chr10:1036000-1040400	Weak transcription	Colon Smooth Muscle	Colon
8	chr10:1036000-1040600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr10:1036000-1040600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr10:1036000-1040800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr10:1036000-1041000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:1036000-1046600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:1036000-1046600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr10:1036000-1048000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr10:1036000-1066800	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr10:1036200-1040600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr10:1036200-1046400	Weak transcription	Fetal Heart	heart
18	chr10:1036200-1061800	Weak transcription	Stomach Mucosa	stomach
19	chr10:1036800-1066000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr10:1036800-1066800	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr10:1036800-1066800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr10:1036800-1066800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr10:1037000-1066000	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr10:1037000-1066200	Strong transcription	H1 Cell Line	embryonic stem cell
25	chr10:1037200-1040000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr10:1037200-1040800	Weak transcription	Gastric	stomach
27	chr10:1037200-1041000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr10:1037200-1042000	Weak transcription	Small Intestine	intestine
29	chr10:1037200-1043600	Weak transcription	Psoas Muscle	Psoas
30	chr10:1037200-1047200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:1037200-1049800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr10:1037200-1066800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr10:1037200-1067200	Strong transcription	NHEK	skin
34	chr10:1037400-1053600	Strong transcription	K562	blood
35	chr10:1038000-1046600	Strong transcription	A549	lung
36	chr10:1038000-1054000	Strong transcription	Hela-S3	cervix
37	chr10:1038000-1066200	Strong transcription	HUVEC	blood vessel
38	chr10:1038000-1066200	Strong transcription	Osteobl	bone
39	chr10:1038000-1067200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr10:1038200-1048200	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr10:1038200-1067000	Strong transcription	HSMM	muscle
42	chr10:1038200-1067200	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr10:1038200-1067400	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr10:1038400-1039800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:1038400-1039800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr10:1038400-1039800	Strong transcription	Fetal Brain Female	brain
47	chr10:1038400-1040000	Genic enhancers	Adipose Nuclei	Adipose
48	chr10:1038400-1040200	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr10:1038400-1042400	Strong transcription	Fetal Lung	lung
50	chr10:1038400-1044800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links