Variant report

Variant	rs2645985
Chromosome Location	chr9:115510812-115510813
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:115478146..115483068-chr9:115509233..115514262,7	K562	blood:
2	chr9:115509754..115512033-chr9:115512589..115514776,2	MCF-7	breast:
3	chr9:115496362..115497969-chr9:115509483..115511853,2	K562	blood:
4	chr9:115509069..115511911-chr9:115553211..115555392,2	MCF-7	breast:
5	chr9:115494981..115496599-chr9:115509076..115511385,2	MCF-7	breast:
6	chr9:115509482..115511255-chr9:115511256..115512881,3	K562	blood:
7	chr9:115247555..115250048-chr9:115510709..115513501,2	K562	blood:

Variant related genes	Relation type
ENSG00000165185	Chromatin interaction
ENSG00000148153	Chromatin interaction
ENSG00000148158	Chromatin interaction
ENSG00000230185	Chromatin interaction
ENSG00000226609	Chromatin interaction

Extended variants
information (count: 129 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10115711	1.00[ASN][1000 genomes]
rs10124260	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124979	1.00[ASN][1000 genomes]
rs10733594	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10733598	1.00[ASN][1000 genomes]
rs10733599	1.00[ASN][1000 genomes]
rs10739370	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10739373	1.00[ASN][1000 genomes]
rs10739374	1.00[ASN][1000 genomes]
rs10739376	1.00[ASN][1000 genomes]
rs10759590	1.00[ASN][1000 genomes]
rs10759603	1.00[ASN][1000 genomes]
rs10759604	1.00[ASN][1000 genomes]
rs1158331	1.00[ASN][1000 genomes]
rs11791531	1.00[ASN][1000 genomes]
rs1324931	1.00[ASN][1000 genomes]
rs1361719	0.81[EUR][1000 genomes]
rs1418409	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1539338	1.00[ASN][1000 genomes]
rs1570754	1.00[ASN][1000 genomes]
rs1693411	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1711746	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1711747	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1832890	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1891402	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1891403	0.86[EUR][1000 genomes]
rs1965335	0.92[EUR][1000 genomes]
rs2025544	1.00[ASN][1000 genomes]
rs2051018	1.00[ASN][1000 genomes]
rs2147643	1.00[ASN][1000 genomes]
rs2147646	1.00[ASN][1000 genomes]
rs2153837	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2182048	1.00[ASN][1000 genomes]
rs2185769	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2645991	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2645994	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2796025	1.00[ASN][1000 genomes]
rs2796028	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2796031	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2796035	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2796037	0.85[EUR][1000 genomes]
rs2995805	0.80[EUR][1000 genomes]
rs4246892	1.00[ASN][1000 genomes]
rs4360356	1.00[ASN][1000 genomes]
rs4549852	1.00[ASN][1000 genomes]
rs4604521	0.82[EUR][1000 genomes]
rs4978507	1.00[ASN][1000 genomes]
rs4978510	1.00[ASN][1000 genomes]
rs4979154	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4979155	1.00[ASN][1000 genomes]
rs4979157	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4979165	1.00[ASN][1000 genomes]
rs4979183	1.00[ASN][1000 genomes]
rs4979184	1.00[ASN][1000 genomes]
rs4979186	1.00[ASN][1000 genomes]
rs6477959	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs700122	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7026450	1.00[ASN][1000 genomes]
rs7030795	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7038684	1.00[ASN][1000 genomes]
rs7040954	1.00[ASN][1000 genomes]
rs7041965	1.00[ASN][1000 genomes]
rs7047914	1.00[ASN][1000 genomes]
rs72768411	0.92[EUR][1000 genomes]
rs72768423	0.84[AMR][1000 genomes]
rs7859175	1.00[ASN][1000 genomes]
rs7862183	0.86[EUR][1000 genomes]
rs7869100	1.00[ASN][1000 genomes]
rs786961	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786965	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786966	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786967	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786968	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786969	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786972	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786973	1.00[ASN][1000 genomes]
rs786977	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7872628	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787278	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787281	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787285	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787286	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787287	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787291	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787292	0.92[EUR][1000 genomes]
rs787296	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787299	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787302	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787303	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7873289	1.00[ASN][1000 genomes]
rs885387	1.00[ASN][1000 genomes]
rs912662	1.00[ASN][1000 genomes]
rs9409123	0.93[EUR][1000 genomes]
rs947609	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs980345	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758198	chr9:115240454-116002951	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759710	chr9:115240454-116002951	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv515899	chr9:115359049-115593870	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv34346	chr9:115360505-115581453	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv1038999	chr9:115367078-115590950	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	esv2757350	chr9:115371397-115594108	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
7	nsv471317	chr9:115375153-115558246	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	esv2761275	chr9:115376461-115590962	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv1035169	chr9:115378282-115573581	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription 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 lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1049451	chr9:115378282-115585109	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv1047374	chr9:115378282-115590950	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1038306	chr9:115379305-115595695	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS 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	15 gene(s)	inside rSNPs	diseases
13	nsv540194	chr9:115379305-115595695	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1051909	chr9:115379505-115588377	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv540195	chr9:115379505-115588377	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv915763	chr9:115379600-115588349	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	esv3693040	chr9:115381164-115578065	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv515121	chr9:115383227-115585827	Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
19	nsv1044168	chr9:115383253-115585109	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
20	nsv1048327	chr9:115383253-115589646	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv1044381	chr9:115383253-115590950	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv442163	chr9:115383255-115590578	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
23	esv35051	chr9:115383332-115573581	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
24	esv34763	chr9:115383332-115581453	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
25	nsv430090	chr9:115383445-115594445	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv1041424	chr9:115389428-115590950	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	nsv1050186	chr9:115390759-115550453	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
28	nsv1047625	chr9:115390759-115587347	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
29	nsv540196	chr9:115390759-115587347	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
30	nsv615198	chr9:115397206-115589251	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
31	nsv893733	chr9:115397206-115712068	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
32	nsv1051808	chr9:115397891-115590950	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
33	esv34739	chr9:115409445-115581453	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
34	nsv8559	chr9:115510399-115514319	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115495200-115512400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:115502400-115511200	Weak transcription	Fetal Intestine Small	intestine
3	chr9:115502400-115512000	Weak transcription	Right Atrium	heart
4	chr9:115502800-115511800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr9:115504000-115512000	Weak transcription	Spleen	Spleen
6	chr9:115504200-115511800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr9:115504800-115511800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr9:115505800-115511600	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr9:115506200-115511400	Enhancers	Brain Hippocampus Middle	brain
10	chr9:115506400-115512000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr9:115506600-115512000	Weak transcription	NHLF	lung
12	chr9:115506800-115511600	Weak transcription	Primary B cells from cord blood	blood
13	chr9:115507000-115512200	Weak transcription	HSMMtube	muscle
14	chr9:115507400-115511800	Weak transcription	Fetal Heart	heart
15	chr9:115507400-115512000	Weak transcription	Primary B cells from peripheral blood	blood
16	chr9:115507600-115511000	Weak transcription	Brain Angular Gyrus	brain
17	chr9:115508400-115512000	Weak transcription	Rectal Smooth Muscle	rectum
18	chr9:115508600-115511400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:115508800-115512000	Weak transcription	Fetal Stomach	stomach
20	chr9:115509000-115511800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr9:115509600-115511600	Weak transcription	K562	blood
22	chr9:115509600-115512000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr9:115509600-115512000	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr9:115509800-115511000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr9:115509800-115511600	Enhancers	Brain Substantia Nigra	brain
26	chr9:115509800-115511800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:115509800-115511800	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr9:115510000-115511800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr9:115510000-115511800	Weak transcription	Osteobl	bone
30	chr9:115510000-115512000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:115510000-115512000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr9:115510200-115511000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr9:115510200-115511000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr9:115510400-115511600	Enhancers	GM12878-XiMat	blood
35	chr9:115510400-115512200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr9:115510600-115511400	Enhancers	Primary hematopoietic stem cells	blood
37	chr9:115510600-115511400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr9:115510600-115511800	Enhancers	Brain Anterior Caudate	brain
39	chr9:115510800-115511000	Enhancers	Primary T cells fromperipheralblood	blood
40	chr9:115510800-115511000	Enhancers	Small Intestine	intestine
41	chr9:115510800-115511200	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr9:115510800-115511200	Weak transcription	HepG2	liver
43	chr9:115510800-115511400	Enhancers	Brain Cingulate Gyrus	brain
44	chr9:115510800-115512000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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