Variant report

Variant	rs10230128
Chromosome Location	chr7:105027630-105027631
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No data

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

No.	Distal block	Cell Line	Cell type
1	chr7:104651368..104653205-chr7:105026206..105027848,2	K562	blood:
2	chr7:104653211..104654776-chr7:105027099..105029228,2	K562	blood:
3	chr7:105027174..105029032-chr7:105171146..105173908,2	K562	blood:
4	chr7:104757007..104759673-chr7:105027481..105029991,2	MCF-7	breast:
5	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
6	chr7:104650837..104656019-chr7:105026206..105030997,7	K562	blood:
7	chr7:105019571..105021474-chr7:105027326..105029018,2	MCF-7	breast:
8	chr7:105026529..105029377-chr7:105162488..105165118,2	MCF-7	breast:
9	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
10	chr5:144628686..144629379-chr7:105027367..105028166,2	MCF-7	breast:
11	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:
12	chr7:104715799..104718256-chr7:105026783..105029016,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000239569	Chromatin interaction
ENSG00000135249	Chromatin interaction
ENSG00000091127	Chromatin interaction
ENSG00000005483	Chromatin interaction
ENSG00000228393	Chromatin interaction
ENSG00000135250	Chromatin interaction

Extended variants
information (count: 119 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10224564	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10227302	0.80[ASN][1000 genomes]
rs10228503	0.89[JPT][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10230449	0.93[EUR][1000 genomes]
rs10233695	0.89[EUR][1000 genomes]
rs10235252	0.85[EUR][1000 genomes]
rs10240574	0.85[CHB][hapmap];0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10248422	0.92[CEU][hapmap];0.84[JPT][hapmap];0.91[YRI][hapmap];0.93[EUR][1000 genomes]
rs10248954	0.91[CEU][hapmap];0.84[JPT][hapmap];0.96[YRI][hapmap];0.93[EUR][1000 genomes]
rs10249170	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10252295	0.84[JPT][hapmap];0.85[EUR][1000 genomes]
rs10253496	0.84[EUR][1000 genomes]
rs10255779	0.93[EUR][1000 genomes]
rs10258841	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10259721	0.89[JPT][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10261613	0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10261738	0.81[AMR][1000 genomes]
rs10261782	1.00[CEU][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10267633	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10269989	0.94[JPT][hapmap]
rs10272634	0.93[EUR][1000 genomes]
rs10276153	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10280336	0.90[EUR][1000 genomes]
rs10953473	0.89[JPT][hapmap];0.85[EUR][1000 genomes]
rs11769318	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11769936	0.93[EUR][1000 genomes]
rs11973742	0.91[EUR][1000 genomes]
rs11973780	0.93[EUR][1000 genomes]
rs12537761	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12666949	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12669532	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12705305	0.89[JPT][hapmap];0.85[EUR][1000 genomes]
rs13223001	1.00[CEU][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13237370	0.83[EUR][1000 genomes]
rs13246886	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17721991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17778396	0.93[EUR][1000 genomes]
rs1917047	1.00[CEU][hapmap];0.95[YRI][hapmap];0.90[EUR][1000 genomes]
rs1978201	1.00[CEU][hapmap];0.89[JPT][hapmap];0.85[EUR][1000 genomes]
rs2040913	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2237611	0.80[EUR][1000 genomes]
rs2237615	0.91[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.90[EUR][1000 genomes]
rs2237616	1.00[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.90[EUR][1000 genomes]
rs2237618	0.84[JPT][hapmap];0.84[EUR][1000 genomes]
rs2237619	0.84[JPT][hapmap];0.85[EUR][1000 genomes]
rs2237620	1.00[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.93[EUR][1000 genomes]
rs2286124	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2299312	0.90[EUR][1000 genomes]
rs2299313	1.00[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2299314	0.93[EUR][1000 genomes]
rs2299316	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2299320	1.00[CEU][hapmap];0.95[YRI][hapmap];0.93[EUR][1000 genomes]
rs2299325	0.84[EUR][1000 genomes]
rs2299326	1.00[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.90[EUR][1000 genomes]
rs2385542	0.89[JPT][hapmap]
rs2385556	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28461911	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28823350	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34003298	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34154773	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34387062	0.80[ASN][1000 genomes]
rs34717863	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34789097	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35442357	0.85[EUR][1000 genomes]
rs35757884	0.80[ASN][1000 genomes]
rs35973577	0.90[EUR][1000 genomes]
rs35993922	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3735372	0.93[EUR][1000 genomes]
rs3779208	1.00[CEU][hapmap];0.89[JPT][hapmap];0.89[EUR][1000 genomes]
rs3779209	0.84[EUR][1000 genomes]
rs3801283	1.00[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.93[EUR][1000 genomes]
rs3801999	0.80[ASN][1000 genomes]
rs4610671	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4727622	0.92[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4727623	0.80[CHB][hapmap];0.94[JPT][hapmap]
rs4730078	1.00[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4730082	0.80[ASN][1000 genomes]
rs55796396	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60446665	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62488069	0.83[EUR][1000 genomes]
rs6466064	0.80[ASN][1000 genomes]
rs6971241	0.83[CEU][hapmap];0.89[JPT][hapmap];0.85[EUR][1000 genomes]
rs717352	1.00[CEU][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.93[EUR][1000 genomes]
rs725506	1.00[CEU][hapmap];0.84[JPT][hapmap];0.92[YRI][hapmap];0.93[EUR][1000 genomes]
rs73186027	0.93[EUR][1000 genomes]
rs73188303	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73188305	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7357199	0.80[ASN][1000 genomes]
rs7808168	1.00[CEU][hapmap];0.89[JPT][hapmap];0.87[EUR][1000 genomes]
rs8180735	0.85[EUR][1000 genomes]
rs8180737	1.00[CEU][hapmap];0.84[JPT][hapmap];0.91[YRI][hapmap];0.84[EUR][1000 genomes]
rs9641343	0.89[JPT][hapmap];0.85[EUR][1000 genomes]
rs9641345	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.95[YRI][hapmap]
rs9641347	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9641348	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34588	chr7:104737612-105153242	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv2757233	chr7:104758250-105208492	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	esv2759549	chr7:104758250-105208492	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv8196	chr7:104763559-105155978	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	esv34580	chr7:104763580-105153242	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	esv2758127	chr7:104766707-105110581	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv1028228	chr7:104807207-105182998	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer 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	39 gene(s)	inside rSNPs	diseases
8	nsv932138	chr7:104826194-105152816	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats 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	15 gene(s)	inside rSNPs	diseases
9	nsv1015688	chr7:104849770-105182998	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv1029832	chr7:104905057-105112489	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
11	nsv1023767	chr7:104931143-105190662	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
12	nsv539049	chr7:104931143-105190662	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
13	nsv1034689	chr7:104950564-105085879	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	nsv1022065	chr7:104997315-105190662	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	nsv888929	chr7:105012975-105163091	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
16	nsv888930	chr7:105012975-105170476	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
17	nsv888931	chr7:105012975-105173974	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
18	nsv888932	chr7:105012975-105179756	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
19	nsv888933	chr7:105012975-105193051	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	nsv888934	chr7:105016900-105056010	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
21	esv3436858	chr7:105017550-105044209	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
22	nsv1018975	chr7:105018374-105153618	Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
23	nsv539050	chr7:105018374-105153618	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
24	nsv1023564	chr7:105018484-105182998	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104995200-105028200	Weak transcription	Esophagus	oesophagus
2	chr7:104995400-105028000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:105000000-105028200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:105008200-105028200	Weak transcription	Pancreas	Pancrea
5	chr7:105009200-105028000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:105009200-105028000	Weak transcription	Psoas Muscle	Psoas
7	chr7:105018000-105028000	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr7:105018200-105028000	Weak transcription	Left Ventricle	heart
9	chr7:105018600-105027800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:105018600-105028000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr7:105018800-105027800	Weak transcription	Stomach Mucosa	stomach
12	chr7:105020800-105028000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:105023400-105027800	Weak transcription	Brain Substantia Nigra	brain
14	chr7:105023400-105027800	Weak transcription	Fetal Muscle Trunk	muscle
15	chr7:105025200-105027800	Weak transcription	Fetal Intestine Large	intestine
16	chr7:105025800-105027800	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr7:105025800-105028000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:105026200-105028200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:105026400-105027800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:105026400-105028200	Weak transcription	Gastric	stomach
21	chr7:105026400-105028200	Weak transcription	Spleen	Spleen
22	chr7:105026600-105027800	Enhancers	Primary T cells fromperipheralblood	blood
23	chr7:105026600-105027800	Weak transcription	Fetal Stomach	stomach
24	chr7:105027000-105027800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:105027200-105027800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:105027200-105027800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:105027200-105027800	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr7:105027200-105027800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:105027200-105027800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:105027200-105027800	Enhancers	Adipose Nuclei	Adipose
31	chr7:105027200-105027800	Enhancers	Fetal Brain Female	brain
32	chr7:105027200-105027800	Enhancers	NHEK	skin
33	chr7:105027200-105028000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:105027200-105028000	Enhancers	Primary B cells from peripheral blood	blood
35	chr7:105027200-105028000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr7:105027200-105028000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:105027200-105028000	Enhancers	Fetal Heart	heart
38	chr7:105027200-105028200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr7:105027200-105028200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr7:105027200-105028200	Flanking Active TSS	Dnd41	blood
41	chr7:105027200-105028600	Flanking Active TSS	Primary B cells from cord blood	blood
42	chr7:105027200-105030000	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr7:105027400-105027800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:105027400-105027800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr7:105027400-105027800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr7:105027400-105027800	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr7:105027400-105027800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr7:105027400-105027800	Enhancers	Liver	Liver
49	chr7:105027400-105027800	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:105027400-105027800	Enhancers	Colon Smooth Muscle	Colon

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