Variant report

Variant	rs2303834
Chromosome Location	chr2:179469715-179469716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:179458881..179461701-chr2:179467712..179470922,3	K562	blood:
2	chr2:179463119..179466296-chr2:179467521..179471323,4	K562	blood:
3	chr2:179469607..179471579-chr2:179483428..179486128,2	K562	blood:
4	chr2:179464721..179466289-chr2:179468538..179470638,3	K562	blood:

Variant related genes	Relation type
ENSG00000237298	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs16866391	1.00[GIH][hapmap]
rs2303836	1.00[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834468	chr2:179351116-179533625	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active 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
2	esv2757841	chr2:179409072-179608242	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv2759103	chr2:179409072-179608242	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1000642	chr2:179438866-179503211	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179388800-179495800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:179408000-179503000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:179414800-179471800	Weak transcription	Brain Substantia Nigra	brain
4	chr2:179428400-179478600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr2:179430800-179480000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:179435200-179469800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:179437600-179478800	Weak transcription	Esophagus	oesophagus
8	chr2:179438200-179474800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr2:179438400-179518200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:179440200-179474400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:179440600-179478800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr2:179440600-179494000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr2:179440600-179505200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr2:179441400-179498800	Weak transcription	Brain Anterior Caudate	brain
15	chr2:179441600-179495000	Weak transcription	Fetal Intestine Small	intestine
16	chr2:179441800-179471600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr2:179442000-179484200	Weak transcription	Colonic Mucosa	Colon
18	chr2:179442200-179476800	Weak transcription	Placenta	Placenta
19	chr2:179442600-179475800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:179442600-179478800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr2:179442800-179492000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr2:179442800-179493400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:179443000-179471200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr2:179444800-179484400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr2:179449400-179472600	Weak transcription	Brain Hippocampus Middle	brain
26	chr2:179450000-179482400	Weak transcription	Small Intestine	intestine
27	chr2:179453600-179471200	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr2:179455200-179474200	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr2:179455800-179472600	Strong transcription	Skeletal Muscle Male	skeletal muscle
30	chr2:179458000-179474600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr2:179459000-179479400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:179460800-179480200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr2:179461800-179480400	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr2:179461800-179484000	Weak transcription	Fetal Brain Male	brain
35	chr2:179462200-179470000	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr2:179463800-179492000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr2:179464400-179477600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr2:179464600-179497400	Weak transcription	GM12878-XiMat	blood
39	chr2:179464800-179474400	Weak transcription	Fetal Kidney	kidney
40	chr2:179464800-179476200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:179464800-179477600	Weak transcription	Duodenum Mucosa	Duodenum
42	chr2:179464800-179481600	Weak transcription	Dnd41	blood
43	chr2:179465600-179483600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr2:179465800-179472600	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr2:179465800-179481000	Weak transcription	Colon Smooth Muscle	Colon
46	chr2:179465800-179483200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:179466200-179474600	Weak transcription	Fetal Lung	lung
48	chr2:179466200-179478600	Weak transcription	Brain Cingulate Gyrus	brain
49	chr2:179466200-179480400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:179466200-179484600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links