Variant report

Variant	nsv979148
Chromosome Location	chr2:172373054-172375371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr2:172373745-172373941	T-47D	breast:	n/a	n/a
2	GABPA	chr2:172373908-172374236	HepG2	liver:	n/a	n/a
3	HEY1	chr2:172373849-172374271	HepG2	liver:	n/a	n/a
4	HEY1	chr2:172374008-172374253	HepG2	liver:	n/a	n/a
5	HEY1	chr2:172373679-172374278	K562	blood:	n/a	n/a
6	HEY1	chr2:172373756-172374138	K562	blood:	n/a	n/a
7	MAFK	chr2:172373502-172373513	HepG2	liver:	n/a	n/a
8	MYC	chr2:172374154-172374166	MCF-7	breast:	n/a	n/a
9	POLR2A	chr2:172373936-172373993	A549	lung:	n/a	n/a
10	POLR2A	chr2:172373817-172374218	A549	lung:	n/a	n/a
11	POLR2A	chr2:172373648-172374372	GM12878	blood:	n/a	n/a
12	POLR2A	chr2:172373796-172374244	GM12878	blood:	n/a	n/a
13	POLR2A	chr2:172374009-172374276	A549	lung:	n/a	n/a
14	POLR2A	chr2:172373774-172374248	A549	lung:	n/a	n/a
15	POLR2A	chr2:172373899-172374237	MCF-7	breast:	n/a	n/a
16	POLR2A	chr2:172373927-172374205	HepG2	liver:	n/a	n/a
17	POLR2A	chr2:172373677-172374186	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr2:172373797-172373977	MCF-7	breast:	n/a	n/a
19	POLR2A	chr2:172373700-172374213	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr2:172373796-172374213	HepG2	liver:	n/a	n/a
21	POLR2A	chr2:172373980-172374193	MCF-7	breast:	n/a	n/a
22	POLR2A	chr2:172373611-172374208	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr2:172373682-172373785	HepG2	liver:	n/a	n/a
24	POLR2A	chr2:172373713-172373770	HUVEC	blood vessel:	n/a	n/a
25	POLR2A	chr2:172373836-172374227	A549	lung:	n/a	n/a
26	POLR2A	chr2:172373867-172373885	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr2:172373713-172374217	GM12878	blood:	n/a	n/a
28	POLR2A	chr2:172373839-172374208	A549	lung:	n/a	n/a
29	POLR2A	chr2:172373583-172374271	GM12892	blood:	n/a	n/a
30	POLR2A	chr2:172373921-172374078	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr2:172374060-172374229	MCF-7	breast:	n/a	n/a
32	POLR2A	chr2:172373713-172374029	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr2:172373648-172374333	GM12892	blood:	n/a	n/a
34	POLR2A	chr2:172373851-172374250	GM12878	blood:	n/a	n/a
35	POU2F2	chr2:172373745-172374337	GM12878	blood:	n/a	n/a
36	POU2F2	chr2:172374073-172374248	GM12878	blood:	n/a	n/a
37	REST	chr2:172373835-172374242	SK-N-SH	brain:	n/a	n/a
38	SETDB1	chr2:172373327-172373601	U2OS	brain:	n/a	n/a
39	SIN3AK20	chr2:172374059-172374243	HepG2	liver:	n/a	n/a
40	SPI1	chr2:172373891-172374082	K562	blood:	n/a	n/a
41	TAF1	chr2:172373796-172374248	HepG2	liver:	n/a	n/a
42	TCF12	chr2:172373990-172374265	GM12878	blood:	n/a	n/a
43	TCF3	chr2:172373934-172374310	GM12878	blood:	n/a	n/a
44	ZBTB33	chr2:172373603-172374367	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:172374119-172374169	NB4	blood:	n/a
2	chr2:172374119-172374169	H1-hESC	embryonic stem cell:	embryo
3	chr2:172373923-172373973	PANC-1	pancreas:	n/a
4	chr2:172373923-172373973	SAEC	small airway:	n/a
5	chr2:172374119-172374169	Jurkat	blood:	n/a
6	chr2:172373923-172373973	AG09309	skin:	n/a
7	chr2:172373923-172373973	AG10803	skin:	n/a
8	chr2:172373923-172373973	PFSK-1	brain:	n/a
9	chr2:172373923-172373973	HRCEpiC	kidney:	n/a
10	chr2:172374119-172374169	ovcar-3	ovarian:	n/a
11	chr2:172373923-172373973	NHBE	bronchial:	n/a
12	chr2:172374119-172374169	Hepatocyte	liver:	n/a
13	chr2:172373923-172373973	NT2-D1	testis:	n/a
14	chr2:172373923-172373973	SKMC	muscle:	n/a
15	chr2:172373923-172373973	SK-N-SH	brain:	n/a
16	chr2:172374119-172374169	HEK293	kidney:	embryo
17	chr2:172373923-172373973	HepG2	liver:	n/a
18	chr2:172373923-172373973	BJ	skin:	n/a
19	chr2:172374119-172374169	IMR90	lung:	fetal
20	chr2:172374169-172374219	NB4	blood:	n/a
21	chr2:172373923-172373973	SK-N-MC	brain:	n/a
22	chr2:172374169-172374219	A549	lung:	n/a
23	chr2:172373923-172373973	HAEpiC	amniotic membrane:	n/a
24	chr2:172374169-172374219	GM12892	blood:	n/a
25	chr2:172374119-172374169	HL-60	blood:	n/a
26	chr2:172374119-172374169	A549	lung:	n/a
27	chr2:172374169-172374219	HCF	heart:	n/a
28	chr2:172374169-172374219	PFSK-1	brain:	n/a
29	chr2:172374119-172374169	U87	brain:	n/a
30	chr2:172373923-172373973	RPTEC	kidney:	n/a
31	chr2:172373923-172373973	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:172374119-172374169	RPTEC	kidney:	n/a
33	chr2:172373923-172373973	H1-hESC	embryonic stem cell:	embryo
34	chr2:172373923-172373973	T-47D	breast:	n/a
35	chr2:172373923-172373973	GM19239	blood:	n/a
36	chr2:172374169-172374219	BE2_C	brain:	n/a
37	chr2:172374169-172374219	AoSMC	blood vessel:	n/a
38	chr2:172374169-172374219	CMK	blood:	n/a
39	chr2:172374119-172374169	HNPCEpiC	eye:	n/a
40	chr2:172374119-172374169	NHDF-neo	bronchial:	n/a
41	chr2:172373923-172373973	HCF	heart:	n/a
42	chr2:172373923-172373973	Jurkat	blood:	n/a
43	chr2:172374169-172374219	Caco-2	colon:	n/a
44	chr2:172373923-172373973	PrEC	prostate:	n/a
45	chr2:172374119-172374169	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:172374169-172374219	NHDF-neo	bronchial:	n/a
47	chr2:172374119-172374169	HMEC	breast:	n/a
48	chr2:172374119-172374169	PrEC	prostate:	n/a
49	chr2:172374119-172374169	GM06990	blood:	n/a
50	chr2:172374169-172374219	SK-N-SH	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:172370595..172374063-chr2:172374486..172376934,3	MCF-7	breast:
2	chr2:172288399..172297381-chr2:172370978..172381493,22	K562	blood:
3	chr2:172370595..172374063-chr2:172374486..172376934,3	MCF-7	breast:
4	chr2:172340109..172342065-chr2:172370654..172373620,2	K562	blood:
5	chr2:172374965..172377030-chr2:172379284..172381375,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000233762	TF binding region
CYBRD1	TF binding region
ENSG00000233762	CpG island
CYBRD1	CpG island
ENSG00000123600	chromatin interactions
ENSG00000115827	chromatin interactions
ENSG00000071967	chromatin interactions

Extended variants
information (count: 120 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:120 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554299648	chr2:172373130-172373131	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs566077355	chr2:172373132-172373133	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189124991	chr2:172373242-172373243	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs202144876	chr2:172373271-172373272	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs5836341	chr2:172373273-172373274	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs397873268	chr2:172373274-172373275	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs76739758	chr2:172373335-172373336	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
8	rs541790833	chr2:172373353-172373354	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs576394050	chr2:172373373-172373374	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs57826998	chr2:172373425-172373426	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs374428194	chr2:172373458-172373459	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs555684847	chr2:172373484-172373485	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs1476110	chr2:172373507-172373508	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs374332745	chr2:172373509-172373510	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs181024930	chr2:172373519-172373520	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs560169696	chr2:172373520-172373521	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs148032138	chr2:172373535-172373536	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs545900420	chr2:172373596-172373597	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549586124	chr2:172373597-172373598	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141793514	chr2:172373603-172373604	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185392208	chr2:172373608-172373609	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs146358443	chr2:172373631-172373632	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550097342	chr2:172373665-172373666	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs558408991	chr2:172373667-172373668	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371392064	chr2:172373703-172373704	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs568405417	chr2:172373705-172373706	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529085183	chr2:172373724-172373725	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs200342981	chr2:172373732-172373733	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs188688071	chr2:172373761-172373762	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs565881707	chr2:172373786-172373787	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs150577215	chr2:172373799-172373800	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs202149263	chr2:172373805-172373806	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs181429618	chr2:172373825-172373826	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs113051268	chr2:172373843-172373844	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs555623039	chr2:172373864-172373865	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs574020085	chr2:172373881-172373882	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs541349303	chr2:172373913-172373914	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs553258638	chr2:172373919-172373920	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs578133345	chr2:172373924-172373925	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs138537929	chr2:172373963-172373964	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs564254721	chr2:172373981-172373982	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs576097523	chr2:172373984-172373985	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs543478741	chr2:172373993-172373994	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs6433295	chr2:172374000-172374001	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
45	rs186858760	chr2:172374001-172374002	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs547677934	chr2:172374017-172374018	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs559236249	chr2:172374043-172374044	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs6433296	chr2:172374078-172374079	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
49	rs139230888	chr2:172374108-172374109	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs570164382	chr2:172374111-172374112	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:47)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172367000-172378000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:172370800-172373400	Weak transcription	Fetal Thymus	thymus
3	chr2:172370800-172378400	Weak transcription	Right Ventricle	heart
4	chr2:172371200-172376200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:172371600-172375800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr2:172371600-172376400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr2:172372000-172373200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr2:172372000-172373200	Enhancers	Osteobl	bone
9	chr2:172372000-172373400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:172372000-172373600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:172372000-172373600	Enhancers	NHDF-Ad	bronchial
12	chr2:172372200-172373200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:172372200-172373400	Enhancers	HSMM	muscle
14	chr2:172372200-172373600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:172372200-172373600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:172372200-172373600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr2:172372200-172373600	Enhancers	NH-A	brain
18	chr2:172372400-172373200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr2:172372400-172373400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr2:172372400-172376200	Weak transcription	GM12878-XiMat	blood
21	chr2:172372400-172376400	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr2:172372600-172373400	Weak transcription	HSMMtube	muscle
23	chr2:172372600-172373600	Enhancers	K562	blood
24	chr2:172372600-172374000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr2:172372800-172373400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr2:172372800-172373600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:172372800-172373600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr2:172373000-172373400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:172373000-172373600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:172373000-172373600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:172373000-172378000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:172373200-172378200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:172373200-172378200	Weak transcription	Osteobl	bone
34	chr2:172373400-172373600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr2:172373400-172373600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr2:172373400-172373600	Enhancers	Fetal Muscle Leg	muscle
37	chr2:172373400-172373600	Bivalent/Poised TSS	Placenta	Placenta
38	chr2:172373400-172373600	Enhancers	HSMMtube	muscle
39	chr2:172373400-172373800	ZNF genes & repeats	Fetal Thymus	thymus
40	chr2:172373400-172377600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr2:172373400-172378000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr2:172373400-172378000	Weak transcription	HSMM	muscle
43	chr2:172373600-172373800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:172373600-172374400	Active TSS	Placenta	Placenta
45	chr2:172373600-172375800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:172373600-172375800	Weak transcription	HSMMtube	muscle
47	chr2:172373600-172375800	Weak transcription	K562	blood
48	chr2:172373600-172377800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr2:172373600-172377800	Weak transcription	NHDF-Ad	bronchial
50	chr2:172373600-172378000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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