Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:196244654..196246787-chr1:196249924..196252778,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10801540	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs10801541	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs10801542	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs1416963	1.00[AMR][1000 genomes]
rs16839768	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16839769	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16839916	1.00[AMR][1000 genomes]
rs1925321	0.82[YRI][hapmap]
rs2335902	1.00[AMR][1000 genomes]
rs4607811	1.00[AMR][1000 genomes]
rs60840993	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs631216	0.88[YRI][hapmap]
rs6413932	1.00[AMR][1000 genomes]
rs6413933	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs6657157	1.00[AMR][1000 genomes]
rs6696031	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065815	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065832	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065849	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7511869	1.00[AMR][1000 genomes]
rs7552572	1.00[AMR][1000 genomes]
rs977157	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872952	chr1:196174790-196304223	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv548741	chr1:196186750-196293493	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv832237	chr1:196205674-196328500	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196234800-196252200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:196234800-196255400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr1:196237000-196253600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:196237200-196253800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:196240000-196252200	Weak transcription	Fetal Lung	lung
6	chr1:196240200-196252000	Weak transcription	Fetal Stomach	stomach
7	chr1:196242600-196251800	Strong transcription	Liver	Liver
8	chr1:196243200-196253600	Weak transcription	Fetal Muscle Leg	muscle
9	chr1:196244600-196272400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr1:196247400-196252400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr1:196248600-196251800	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:196248600-196252200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:196249200-196281400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:196250200-196254000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:196250600-196258400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:196250800-196252600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr1:196250800-196255400	Weak transcription	Ovary	ovary
18	chr1:196250800-196271600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:196251000-196271600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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