Variant report

Variant	rs398051630
Chromosome Location	chr3:17316600-17316601
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876589	chr3:17230884-17346355	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv876590	chr3:17230884-17604963	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS 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	3 gene(s)	inside rSNPs	diseases
3	esv2755406	chr3:17237396-17589896	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv876591	chr3:17246392-17671992	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv3388594	chr3:17315948-17319746	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2021166	chr3:17316599-17316600	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv1084265	chr3:17316599-17316600	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17250000-17330200	Weak transcription	Aorta	Aorta
2	chr3:17255200-17363800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:17273600-17330200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:17277600-17328600	Weak transcription	Primary T cells from cord blood	blood
5	chr3:17279400-17330200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr3:17279800-17329600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:17296600-17330200	Weak transcription	Left Ventricle	heart
8	chr3:17298800-17373000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr3:17301400-17335400	Weak transcription	Ovary	ovary
10	chr3:17307400-17321800	Weak transcription	Fetal Intestine Small	intestine
11	chr3:17311000-17330400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr3:17313600-17320800	Weak transcription	Primary B cells from cord blood	blood
13	chr3:17313800-17332200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr3:17315000-17332400	Weak transcription	GM12878-XiMat	blood
15	chr3:17315200-17321800	Weak transcription	Gastric	stomach
16	chr3:17315800-17330200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:17316000-17321400	Weak transcription	Primary B cells from peripheral blood	blood
18	chr3:17316200-17330200	Weak transcription	Fetal Intestine Large	intestine

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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