Variant report

Variant	rs7101638
Chromosome Location	chr11:120504845-120504846
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:120501095..120503196-chr11:120504558..120506204,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10160371	1.00[AMR][1000 genomes]
rs10160449	1.00[AMR][1000 genomes]
rs11217914	1.00[AMR][1000 genomes]
rs12273151	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12294271	1.00[AMR][1000 genomes]
rs12295742	1.00[AMR][1000 genomes]
rs17124128	1.00[EUR][1000 genomes]
rs4590879	1.00[AMR][1000 genomes]
rs7104127	1.00[AMR][1000 genomes]
rs7932311	1.00[AMR][1000 genomes]

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	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv468881	chr11:120446830-120551100	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv556476	chr11:120446830-120551100	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120484800-120507400	Weak transcription	Right Atrium	heart
2	chr11:120498800-120505000	Weak transcription	Fetal Intestine Large	intestine
3	chr11:120503200-120506400	Enhancers	Fetal Brain Male	brain
4	chr11:120503400-120506800	Enhancers	GM12878-XiMat	blood
5	chr11:120503800-120505400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:120504200-120505400	Enhancers	Brain Germinal Matrix	brain
7	chr11:120504200-120505800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr11:120504200-120506800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:120504400-120505000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:120504400-120505200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:120504400-120505400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr11:120504400-120505400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr11:120504400-120506000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr11:120504400-120506200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:120504400-120506200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:120504600-120505000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr11:120504600-120505000	Bivalent Enhancer	Fetal Stomach	stomach
18	chr11:120504600-120505200	Enhancers	Fetal Lung	lung
19	chr11:120504600-120505200	Enhancers	Spleen	Spleen
20	chr11:120504600-120505400	Enhancers	Primary hematopoietic stem cells	blood
21	chr11:120504600-120506200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:120504600-120506200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:120504600-120506400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:120504600-120506400	Enhancers	Fetal Brain Female	brain
25	chr11:120504800-120505000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr11:120504800-120505400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:120504800-120505600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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