Variant report

Variant	rs541584764
Chromosome Location	chr1:210405653-210405654
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	MAX	chr1:210405600-210406261	A549	lung:	n/a	n/a
2	TAF1	chr1:210405633-210405894	SK-N-SH	brain:	n/a	n/a
3	TCF12	chr1:210405238-210406224	SK-N-SH	brain:	n/a	n/a
4	MAX	chr1:210405418-210406263	SK-N-SH	brain:	n/a	n/a
5	RAD21	chr1:210405448-210405790	SK-N-SH_RA	brain:	n/a	n/a
6	POLR2A	chr1:210405595-210408558	H1-neurons	neurons:	n/a	n/a
7	POLR2A	chr1:210405446-210405878	SK-N-SH	brain:	n/a	n/a
8	HA-E2F1	chr1:210405555-210407854	MCF-7	breast:	n/a	chr1:210405557-210405566 chr1:210406562-210406577 chr1:210405978-210405988 chr1:210405975-210405985 chr1:210406950-210406960 chr1:210406620-210406632 chr1:210407579-210407589 chr1:210406572-210406581
9	PBX3	chr1:210405387-210406376	SK-N-SH	brain:	n/a	n/a
10	MYC	chr1:210405314-210405803	MCF10A-Er-Src	breast:	n/a	n/a
11	EP300	chr1:210405319-210406323	SK-N-SH	brain:	n/a	chr1:210405510-210405524 chr1:210405976-210405985 chr1:210405975-210405991 chr1:210405979-210405988 chr1:210405511-210405525 chr1:210405561-210405570
12	REST	chr1:210405235-210408055	H1-neurons	neurons:	n/a	n/a
13	EP300	chr1:210405323-210405817	SK-N-SH_RA	brain:	n/a	chr1:210405510-210405524 chr1:210405511-210405525 chr1:210405561-210405570
14	FOXP2	chr1:210405435-210405745	SK-N-MC	brain:	n/a	n/a
15	POLR2A	chr1:210405299-210405899	SK-N-MC	brain:	n/a	n/a
16	TCF12	chr1:210405200-210408026	SK-N-SH	brain:	n/a	chr1:210407710-210407720

No.	Distal block	Cell Line	Cell type
1	chr1:210398376..210400495-chr1:210402941..210405832,2	K562	blood:
2	chr1:210404317..210408653-chr1:210545033..210548956,7	MCF-7	breast:
3	chr1:210404553..210406882-chr6:30538400..30541136,2	MCF-7	breast:

Variant related genes	Relation type
SERTAD4	TF binding region
ENSG00000204574	Chromatin interaction
ENSG00000200972	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv8769	chr1:210403509-210564588	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	esv3422029	chr1:210404854-210407702	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv3334541	chr1:210405229-210407377	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210405000-210407400	Active TSS	Stomach Smooth Muscle	stomach
2	chr1:210405000-210407600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr1:210405200-210405800	Enhancers	Placenta	Placenta
4	chr1:210405200-210405800	Flanking Active TSS	HUVEC	blood vessel
5	chr1:210405200-210406400	Active TSS	Duodenum Smooth Muscle	Duodenum
6	chr1:210405200-210406600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:210405200-210407600	Active TSS	NH-A	brain
8	chr1:210405400-210405800	Bivalent Enhancer	Fetal Thymus	thymus
9	chr1:210405400-210406000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:210405400-210406000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
11	chr1:210405400-210406400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:210405400-210406400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:210405400-210406400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
14	chr1:210405400-210406600	Active TSS	Muscle Satellite Cultured Cells	--
15	chr1:210405400-210407600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr1:210405400-210407600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
17	chr1:210405400-210407600	Active TSS	Right Ventricle	heart
18	chr1:210405400-210407800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
19	chr1:210405400-210407800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
20	chr1:210405400-210407800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
21	chr1:210405400-210407800	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr1:210405400-210407800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
23	chr1:210405400-210407800	Active TSS	Colon Smooth Muscle	Colon
24	chr1:210405400-210407800	Active TSS	Rectal Smooth Muscle	rectum
25	chr1:210405400-210408000	Bivalent Enhancer	Fetal Brain Male	brain
26	chr1:210405400-210408000	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr1:210405600-210405800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
28	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
31	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
32	chr1:210405600-210405800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:210405600-210405800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:210405600-210405800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
35	chr1:210405600-210405800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:210405600-210405800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:210405600-210405800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr1:210405600-210405800	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr1:210405600-210405800	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr1:210405600-210405800	Flanking Active TSS	Duodenum Mucosa	Duodenum
43	chr1:210405600-210405800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
45	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
46	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
47	chr1:210405600-210405800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
48	chr1:210405600-210405800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
49	chr1:210405600-210405800	Flanking Active TSS	NHEK	skin
50	chr1:210405600-210406000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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