Variant report

Variant	rs4905561
Chromosome Location	chr14:97355545-97355546
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:97349904..97353834-chr14:97354372..97357371,3	K562	blood:
2	chr14:97352755..97357017-chr14:97358100..97363870,8	K562	blood:
3	chr14:97355083..97357318-chr14:97362370..97365310,3	K562	blood:
4	chr14:97342578..97345123-chr14:97353355..97355905,2	K562	blood:

Variant related genes	Relation type
ENSG00000100749	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11160377	0.95[ASN][1000 genomes]
rs11627455	0.95[ASN][1000 genomes]
rs12101203	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12586511	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12589919	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12590169	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12881995	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12882038	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12887093	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12889255	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12892609	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12893513	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12893711	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12894533	0.92[ASN][1000 genomes]
rs12897588	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2145635	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2145636	0.81[ASN][1000 genomes]
rs2180897	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2224443	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4900346	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4900348	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4900350	0.86[ASN][1000 genomes]
rs4900352	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4900353	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4905548	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4905549	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4905550	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4905551	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4905562	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4905563	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4905567	0.95[ASN][1000 genomes]
rs7158545	0.82[ASN][1000 genomes]
rs749279	0.95[ASN][1000 genomes]
rs764300	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8022152	0.95[ASN][1000 genomes]
rs9323955	0.86[ASN][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	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97294000-97362600	Weak transcription	Spleen	Spleen
2	chr14:97303400-97371600	Weak transcription	Ovary	ovary
3	chr14:97325600-97362000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr14:97331000-97378400	Weak transcription	A549	lung
5	chr14:97341400-97357400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr14:97342800-97367000	Weak transcription	NHEK	skin
7	chr14:97347000-97368200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:97348200-97361400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr14:97348600-97356000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr14:97349200-97359200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr14:97349200-97367200	Weak transcription	Primary B cells from cord blood	blood
12	chr14:97349200-97367600	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr14:97349200-97377400	Weak transcription	Primary T cells from cord blood	blood
14	chr14:97349400-97356600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:97349400-97359000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:97349400-97369200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr14:97353400-97356400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr14:97353600-97355600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr14:97353600-97355600	Weak transcription	Fetal Brain Female	brain
20	chr14:97353800-97356000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:97354000-97356000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:97354000-97360200	Weak transcription	Dnd41	blood
23	chr14:97354200-97356000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr14:97354200-97356000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr14:97354200-97356200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr14:97354600-97355600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:97354600-97355600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr14:97355000-97355800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr14:97355000-97355800	Enhancers	Fetal Heart	heart
30	chr14:97355000-97356600	Weak transcription	Thymus	Thymus
31	chr14:97355200-97356600	Weak transcription	Fetal Thymus	thymus
32	chr14:97355200-97363200	Weak transcription	K562	blood
33	chr14:97355400-97360400	Weak transcription	GM12878-XiMat	blood
34	chr14:97355400-97361000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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