Variant report

Variant	rs17098434
Chromosome Location	chr1:76698112-76698113
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	chr1:76655272..76656892-chr1:76697191..76699562,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10493588	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];0.83[YRI][hapmap];0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12074693	0.87[CEU][hapmap]
rs17098431	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17098457	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58138109	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58686996	0.91[EUR][1000 genomes]
rs59079863	0.80[EUR][1000 genomes]
rs66973173	0.88[EUR][1000 genomes]
rs67584550	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67757470	0.96[EUR][1000 genomes]
rs72675947	0.80[EUR][1000 genomes]

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	nsv870621	chr1:76620313-76997071	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1008763	chr1:76692057-76723417	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1001452	chr1:76692057-76724652	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv546584	chr1:76693367-76721164	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv523526	chr1:76695356-76721164	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76692400-76698200	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr1:76692600-76698200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr1:76692600-76698400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr1:76693800-76698400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:76694200-76700600	Weak transcription	Fetal Stomach	stomach
6	chr1:76694600-76705000	Weak transcription	Primary B cells from cord blood	blood
7	chr1:76695400-76699600	Weak transcription	Psoas Muscle	Psoas
8	chr1:76695600-76699800	Weak transcription	Aorta	Aorta
9	chr1:76695600-76703000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:76695600-76703400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:76695600-76703800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:76695600-76703800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:76695600-76703800	Weak transcription	Brain Hippocampus Middle	brain
14	chr1:76695600-76703800	Weak transcription	Brain Substantia Nigra	brain
15	chr1:76695600-76704200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:76695600-76704200	Weak transcription	Brain Anterior Caudate	brain
17	chr1:76695600-76705000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr1:76695600-76708200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:76695800-76703200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:76697000-76698200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr1:76697000-76703600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:76697000-76703600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:76697000-76708200	Weak transcription	Fetal Lung	lung
24	chr1:76697200-76698400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:76697600-76698400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:76698000-76698400	Enhancers	Fetal Intestine Large	intestine
27	chr1:76698000-76698400	Enhancers	Spleen	Spleen
28	chr1:76698000-76699000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:76698000-76699600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr1:76698000-76699600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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