Variant report

Variant	rs182172609
Chromosome Location	chr10:97207785-97207786
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3497577	chr10:97206312-97209110	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3362042	chr10:97206913-97208120	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
3	esv9481	chr10:97206919-97208254	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
4	esv3319851	chr10:97206921-97208124	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv3497576	chr10:97206950-97208089	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
6	esv3319863	chr10:97206984-97208018	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
7	nsv512178	chr10:97206985-97210791	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3497579	chr10:97206996-97208077	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
9	esv3497580	chr10:97207000-97208077	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
10	esv5409	chr10:97207012-97208165	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
11	esv3388258	chr10:97207016-97208047	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
12	esv3319874	chr10:97207041-97208032	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
13	esv3497578	chr10:97207051-97208031	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
14	esv3319885	chr10:97207055-97208029	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
15	esv3497581	chr10:97207055-97208029	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97171000-97208000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr10:97190800-97208200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr10:97193400-97210800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr10:97193800-97208000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:97200200-97208800	Enhancers	Colon Smooth Muscle	Colon
6	chr10:97202800-97209200	Enhancers	Fetal Muscle Leg	muscle
7	chr10:97203200-97208400	Enhancers	Liver	Liver
8	chr10:97203800-97209400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr10:97204000-97208600	Enhancers	Left Ventricle	heart
10	chr10:97204600-97208200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr10:97204600-97208200	Enhancers	Placenta	Placenta
12	chr10:97204600-97208200	Enhancers	Lung	lung
13	chr10:97204600-97208600	Enhancers	Adipose Nuclei	Adipose
14	chr10:97204600-97208600	Enhancers	Fetal Stomach	stomach
15	chr10:97204600-97208800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr10:97204800-97208200	Enhancers	Fetal Lung	lung
17	chr10:97204800-97208600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:97204800-97209200	Enhancers	Right Atrium	heart
19	chr10:97204800-97209200	Enhancers	Right Ventricle	heart
20	chr10:97205000-97208200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr10:97205200-97211000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr10:97205400-97208000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr10:97205600-97207800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr10:97205600-97208200	Enhancers	HUVEC	blood vessel
25	chr10:97205600-97209000	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr10:97205600-97210200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr10:97205800-97208200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:97206000-97207800	Weak transcription	Duodenum Mucosa	Duodenum
29	chr10:97206000-97207800	Weak transcription	HSMMtube	muscle
30	chr10:97206000-97208000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:97206000-97208800	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr10:97206000-97210800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr10:97206000-97210800	Weak transcription	Brain Anterior Caudate	brain
34	chr10:97206000-97210800	Weak transcription	Fetal Brain Male	brain
35	chr10:97206000-97217000	Weak transcription	Gastric	stomach
36	chr10:97206000-97220000	Enhancers	Rectal Smooth Muscle	rectum
37	chr10:97206200-97208000	Weak transcription	NHEK	skin
38	chr10:97206200-97208200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr10:97206200-97208200	Weak transcription	HMEC	breast
40	chr10:97206200-97208600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr10:97206200-97210800	Enhancers	Fetal Heart	heart
42	chr10:97206200-97219000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr10:97206400-97208200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr10:97206600-97207800	Weak transcription	Small Intestine	intestine
45	chr10:97206600-97207800	Weak transcription	K562	blood
46	chr10:97206600-97208200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr10:97206600-97208400	Enhancers	Psoas Muscle	Psoas
48	chr10:97206600-97208600	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr10:97206600-97211000	Weak transcription	Fetal Intestine Large	intestine
50	chr10:97206600-97211400	Weak transcription	Fetal Intestine Small	intestine

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