Variant report

Variant	rs1442137
Chromosome Location	chr4:90818857-90818858
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:90818661-90820935	HUVEC	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:90817680..90820518-chr4:90823255..90825762,2	K562	blood:

Variant related genes	Relation type
MMRN1	TF binding region

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10002435	0.85[CHB][hapmap]
rs10014396	0.81[CHB][hapmap]
rs1442141	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17016168	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs17016183	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs17016190	1.00[CEU][hapmap]
rs17016255	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs17016279	0.82[EUR][1000 genomes]
rs17016316	0.91[AFR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17016326	1.00[AFR][1000 genomes]
rs2035268	1.00[CEU][hapmap];0.81[CHB][hapmap];0.81[LWK][hapmap]
rs3756055	1.00[CEU][hapmap]
rs3756056	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3756057	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3775443	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3775446	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3775447	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3775448	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3775461	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3889916	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3889917	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs3906824	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs59718120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62304971	0.82[EUR][1000 genomes]
rs62304974	0.82[EUR][1000 genomes]
rs6812172	1.00[ASW][hapmap];0.87[YRI][hapmap]
rs6829514	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs7676702	0.82[EUR][1000 genomes]
rs7684637	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs7684892	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs7689942	1.00[CEU][hapmap];0.81[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830400	chr4:90085456-90922432	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv997700	chr4:90791866-90920021	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv830005	chr4:90799398-90963420	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90815800-90820600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:90816400-90822200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:90816600-90819200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr4:90816600-90819400	Active TSS	HUVEC	blood vessel
5	chr4:90816600-90819600	Weak transcription	Spleen	Spleen
6	chr4:90816800-90819400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr4:90816800-90819600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:90817200-90819600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:90817200-90819600	Weak transcription	Fetal Thymus	thymus
10	chr4:90817400-90819200	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr4:90817400-90819200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr4:90817400-90819400	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr4:90817400-90819400	Weak transcription	Primary B cells from cord blood	blood
14	chr4:90817400-90819400	Weak transcription	GM12878-XiMat	blood
15	chr4:90817400-90820000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr4:90817400-90823200	Enhancers	Dnd41	blood
17	chr4:90817800-90822200	Enhancers	Primary T cells from cord blood	blood
18	chr4:90818000-90819200	Weak transcription	Fetal Intestine Small	intestine
19	chr4:90818600-90819000	Active TSS	Primary hematopoietic stem cells	blood
20	chr4:90818800-90819000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr4:90818800-90822400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:90818800-90823200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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