The 2.0 version of rSNPBase

Variant report

Variant rs10176506
Chromosome Location chr2:190646511-190646512
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:126 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190627800-190648200 Weak transcription Gastric stomach
2 chr2:190628200-190648000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr2:190628200-190648000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr2:190628200-190648200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr2:190628400-190648000 Weak transcription ES-WA7 Cell Line embryonic stem cell
6 chr2:190628600-190647000 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr2:190628600-190647200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr2:190628600-190647200 Weak transcription Stomach Mucosa stomach
9 chr2:190628600-190648400 Weak transcription Small Intestine intestine
10 chr2:190629000-190647200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr2:190629800-190647000 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr2:190630000-190646600 Strong transcription Primary hematopoietic stem cells short term culture blood
13 chr2:190630800-190647000 Strong transcription HSMM muscle
14 chr2:190631200-190647200 Strong transcription Fetal Thymus thymus
15 chr2:190631400-190646800 Strong transcription Primary Natural Killer cells fromperipheralblood blood
16 chr2:190631600-190647000 Strong transcription HUES64 Cell Line embryonic stem cell
17 chr2:190632000-190646600 Strong transcription Placenta Placenta
18 chr2:190632800-190647200 Strong transcription Primary B cells from peripheral blood blood
19 chr2:190633200-190646800 Strong transcription HMEC breast
20 chr2:190633600-190646600 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
21 chr2:190634000-190647000 Strong transcription Osteobl bone
22 chr2:190634200-190647400 Strong transcription Fetal Muscle Trunk muscle
23 chr2:190634600-190646600 Strong transcription Muscle Satellite Cultured Cells --
24 chr2:190634600-190647000 Strong transcription NH-A brain
25 chr2:190634600-190647200 Strong transcription H1 Cell Line embryonic stem cell
26 chr2:190634600-190647200 Strong transcription HUES48 Cell Line embryonic stem cell
27 chr2:190634600-190647200 Strong transcription iPS-20b Cell Line embryonic stem cell
28 chr2:190635000-190647000 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
29 chr2:190635000-190647200 Strong transcription iPS-18 Cell Line embryonic stem cell
30 chr2:190635200-190647200 Strong transcription HUES6 Cell Line embryonic stem cell
31 chr2:190636200-190646800 Strong transcription Skeletal Muscle Female skeletal muscle
32 chr2:190636400-190647000 Weak transcription Aorta Aorta
33 chr2:190638200-190647000 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
34 chr2:190640200-190647200 Weak transcription Placenta Amnion Placenta Amnion
35 chr2:190641200-190647000 Weak transcription Rectal Smooth Muscle rectum
36 chr2:190641600-190647200 Strong transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
37 chr2:190641800-190648000 Weak transcription Colonic Mucosa Colon
38 chr2:190642200-190647000 Weak transcription K562 blood
39 chr2:190642600-190647000 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
40 chr2:190642800-190647000 Weak transcription Hela-S3 cervix
41 chr2:190643200-190647200 Strong transcription Fetal Muscle Leg muscle
42 chr2:190643600-190647600 Genic enhancers Primary T helper naive cells from peripheral blood blood
43 chr2:190643800-190647000 Strong transcription A549 lung
44 chr2:190644000-190646800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
45 chr2:190644000-190647000 Genic enhancers Primary T helper cells PMA-I stimulated --
46 chr2:190644000-190647200 Genic enhancers Primary T helper cells fromperipheralblood blood
47 chr2:190644000-190648200 Weak transcription Esophagus oesophagus
48 chr2:190644000-190648200 Weak transcription Spleen Spleen
49 chr2:190644200-190647000 Weak transcription Fetal Stomach stomach
50 chr2:190644200-190647000 Genic enhancers Dnd41 blood

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Last update: Aug 31, 2015