Variant report

Variant	rs555522877
Chromosome Location	chr7:99821533-99821534
allele	-/A
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	chr7:99821139-99821796	GM12878	blood:	n/a	n/a
2	POLR2A	chr7:99820932-99821837	GM12878	blood:	n/a	n/a
3	POLR2A	chr7:99816142-99821987	GM12892	blood:	n/a	n/a
4	POLR2A	chr7:99816171-99821984	GM12892	blood:	n/a	n/a
5	POLR2A	chr7:99816169-99821811	GM12878	blood:	n/a	n/a
6	POLR2A	chr7:99820935-99821862	GM12878	blood:	n/a	n/a
7	POLR2A	chr7:99820884-99821817	GM12892	blood:	n/a	n/a
8	POLR2A	chr7:99820891-99821938	GM12891	blood:	n/a	n/a
9	POLR2A	chr7:99820880-99821913	GM12891	blood:	n/a	n/a
10	POLR2A	chr7:99820790-99821961	GM12892	blood:	n/a	n/a
11	POLR2A	chr7:99820965-99821871	GM12891	blood:	n/a	n/a
12	POLR2A	chr7:99816181-99824845	GM12878	blood:	n/a	n/a
13	POLR2A	chr7:99820825-99821828	GM12891	blood:	n/a	n/a
14	POLR2A	chr7:99821036-99821728	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:99816172..99818771-chr7:99820736..99823098,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000239521	TF binding region
ENSG00000222482	TF binding region
ENSG00000213413	Chromatin interaction
ENSG00000222482	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534298	chr7:99478011-99886076	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1132 gene(s)	inside rSNPs	diseases
2	esv1798486	chr7:99689883-99930879	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1085 gene(s)	inside rSNPs	diseases
3	esv1833059	chr7:99689883-99930879	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1085 gene(s)	inside rSNPs	diseases
4	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
5	nsv427794	chr7:99750981-99960900	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
6	nsv428180	chr7:99750981-99960900	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
7	nsv8182	chr7:99799816-99879781	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv888774	chr7:99807265-99951315	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	esv16057	chr7:99809377-99937347	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
10	esv3379367	chr7:99811760-99938687	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
11	esv3379649	chr7:99812207-99939196	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
12	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
13	esv3358931	chr7:99816130-99943645	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
14	esv3405423	chr7:99816156-99943860	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
15	esv3508070	chr7:99816206-99943813	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
16	esv3508071	chr7:99816206-99943813	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
17	nsv970560	chr7:99821528-99832022	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99801400-99826000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:99807200-99828400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:99807200-99847000	Weak transcription	Fetal Kidney	kidney
4	chr7:99809200-99834800	Weak transcription	HSMMtube	muscle
5	chr7:99810600-99864000	Weak transcription	Right Atrium	heart
6	chr7:99811400-99828600	Weak transcription	HepG2	liver
7	chr7:99811600-99823800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:99811600-99834800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:99812200-99823800	Weak transcription	Stomach Mucosa	stomach
10	chr7:99812400-99839600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:99813800-99825000	Weak transcription	Psoas Muscle	Psoas
12	chr7:99813800-99829400	Weak transcription	Colon Smooth Muscle	Colon
13	chr7:99813800-99838800	Weak transcription	Fetal Brain Male	brain
14	chr7:99813800-99841200	Weak transcription	Left Ventricle	heart
15	chr7:99813800-99846800	Weak transcription	Ovary	ovary
16	chr7:99815000-99828200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr7:99815200-99828800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr7:99815400-99825600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:99815400-99834800	Weak transcription	A549	lung
20	chr7:99815400-99834800	Weak transcription	Osteobl	bone
21	chr7:99815600-99835200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:99815600-99844800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:99815800-99839600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr7:99816400-99823000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr7:99816600-99826400	Strong transcription	Fetal Brain Female	brain
26	chr7:99816600-99827600	Weak transcription	Aorta	Aorta
27	chr7:99816800-99822000	Strong transcription	Brain Angular Gyrus	brain
28	chr7:99816800-99822000	Strong transcription	Brain Substantia Nigra	brain
29	chr7:99816800-99822200	Strong transcription	Brain Hippocampus Middle	brain
30	chr7:99816800-99822600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:99816800-99823200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr7:99816800-99823200	Strong transcription	Brain Cingulate Gyrus	brain
33	chr7:99816800-99823600	Strong transcription	Fetal Stomach	stomach
34	chr7:99816800-99824800	Strong transcription	Brain Germinal Matrix	brain
35	chr7:99816800-99825200	Strong transcription	Brain Inferior Temporal Lobe	brain
36	chr7:99816800-99832000	Strong transcription	Fetal Intestine Small	intestine
37	chr7:99817000-99821600	Strong transcription	Lung	lung
38	chr7:99817000-99824200	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr7:99817000-99824200	Strong transcription	Fetal Muscle Trunk	muscle
40	chr7:99817400-99822600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:99817400-99822600	Strong transcription	Pancreas	Pancrea
42	chr7:99817600-99821800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:99817600-99822600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr7:99818000-99821600	Strong transcription	Brain Anterior Caudate	brain
45	chr7:99818000-99830400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:99818200-99821800	Strong transcription	Adipose Nuclei	Adipose
47	chr7:99818200-99822000	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
48	chr7:99818200-99822000	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr7:99818400-99821800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:99818400-99822600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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