Variant report

Variant	nsv1009550
Chromosome Location	chr3:109577315-109795453
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:749)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr3:109645877-109646527	A549	lung:	n/a	n/a
2	BRCA1	chr3:109791375-109791445	GM12878	blood:	n/a	n/a
3	BRCA1	chr3:109645781-109646410	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr3:109645772-109646547	HCT-116	colon:	n/a	n/a
5	CBX3	chr3:109645702-109646599	HCT-116	colon:	n/a	n/a
6	CBX3	chr3:109609851-109610221	HCT-116	colon:	n/a	n/a
7	CBX3	chr3:109746170-109746640	HCT-116	colon:	n/a	n/a
8	CEBPB	chr3:109641108-109641558	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr3:109645994-109646413	A549	lung:	n/a	n/a
10	CEBPB	chr3:109735169-109735419	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr3:109746103-109746716	HCT-116	colon:	n/a	n/a
12	CEBPB	chr3:109704716-109705062	HepG2	liver:	n/a	chr3:109704857-109704868 chr3:109704856-109704869
13	CEBPB	chr3:109658871-109659190	HepG2	liver:	n/a	chr3:109659035-109659046
14	CEBPB	chr3:109788690-109789314	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:109746236-109746657	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:109738237-109738590	A549	lung:	n/a	n/a
17	CEBPB	chr3:109645987-109646493	A549	lung:	n/a	n/a
18	CEBPB	chr3:109713012-109713264	HepG2	liver:	n/a	chr3:109713148-109713159
19	CEBPB	chr3:109735063-109735497	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr3:109713806-109714074	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:109658867-109659228	IMR90	lung:	n/a	chr3:109659035-109659046
22	CEBPB	chr3:109723207-109723552	Hela-S3	cervix:	n/a	chr3:109723414-109723427 chr3:109723416-109723427
23	CEBPB	chr3:109713603-109714246	HCT-116	colon:	n/a	n/a
24	CEBPB	chr3:109738243-109738606	IMR90	lung:	n/a	n/a
25	CEBPB	chr3:109704716-109705195	Hela-S3	cervix:	n/a	chr3:109704857-109704868 chr3:109704856-109704869
26	CEBPB	chr3:109787020-109787302	IMR90	lung:	n/a	chr3:109787158-109787169
27	CEBPB	chr3:109738296-109738584	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:109746303-109746587	A549	lung:	n/a	n/a
29	CEBPB	chr3:109735150-109735461	A549	lung:	n/a	n/a
30	CEBPB	chr3:109781645-109781922	A549	lung:	n/a	n/a
31	CEBPB	chr3:109645841-109646611	A549	lung:	n/a	n/a
32	CEBPB	chr3:109645773-109646686	HCT-116	colon:	n/a	n/a
33	CEBPB	chr3:109645968-109646417	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr3:109738325-109738600	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr3:109646013-109646487	IMR90	lung:	n/a	n/a
36	CEBPB	chr3:109738259-109738572	HepG2	liver:	n/a	n/a
37	CEBPB	chr3:109671813-109672133	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:109645998-109646461	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:109713605-109714129	HCT-116	colon:	n/a	n/a
40	CEBPB	chr3:109735077-109735599	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:109746256-109746644	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:109619469-109620040	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:109786998-109787264	HepG2	liver:	n/a	chr3:109787158-109787169
44	CEBPB	chr3:109735132-109735448	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr3:109658912-109659180	K562	blood:	n/a	chr3:109659035-109659046
46	CEBPB	chr3:109658937-109659071	H1-hESC	embryonic stem cell:	n/a	chr3:109659035-109659046
47	CEBPB	chr3:109704863-109704976	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr3:109746219-109746575	HCT-116	colon:	n/a	n/a
49	CEBPB	chr3:109651046-109651296	A549	lung:	n/a	n/a
50	CEBPB	chr3:109658874-109659211	A549	lung:	n/a	chr3:109659035-109659046

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:109735618-109735668	ECC-1	luminal epithelium:	n/a
2	chr3:109735618-109735668	HMEC	breast:	n/a
3	chr3:109645423-109645473	GM12878	blood:	n/a
4	chr3:109735618-109735668	NB4	blood:	n/a
5	chr3:109735618-109735668	HUVEC	blood vessel:	n/a
6	chr3:109735618-109735668	HL-60	blood:	n/a
7	chr3:109645423-109645473	LNCaP	prostate:	n/a
8	chr3:109735618-109735668	U87	brain:	n/a
9	chr3:109645423-109645473	HIPEpiC	eye:	n/a
10	chr3:109735618-109735668	GM19239	blood:	n/a
11	chr3:109645423-109645473	RPTEC	kidney:	n/a
12	chr3:109735618-109735668	IMR90	lung:	fetal
13	chr3:109645423-109645473	H1-hESC	embryonic stem cell:	embryo
14	chr3:109645423-109645473	AoSMC	blood vessel:	n/a
15	chr3:109735618-109735668	Hela-S3	cervix:	n/a
16	chr3:109645423-109645473	CMK	blood:	n/a
17	chr3:109645423-109645473	SK-N-SH_RA	brain:	n/a
18	chr3:109735618-109735668	HEEpiC	esophagus:	n/a
19	chr3:109645423-109645473	T-47D	breast:	n/a
20	chr3:109645423-109645473	HEEpiC	esophagus:	n/a
21	chr3:109645423-109645473	GM19239	blood:	n/a
22	chr3:109645423-109645473	PFSK-1	brain:	n/a
23	chr3:109645423-109645473	ProgFib	skin:	n/a
24	chr3:109645423-109645473	IMR90	lung:	fetal
25	chr3:109735618-109735668	SKMC	muscle:	n/a
26	chr3:109735618-109735668	BJ	skin:	n/a
27	chr3:109645423-109645473	MCF10A-Er-Src	breast:	n/a
28	chr3:109735618-109735668	AG09319	gingival:	n/a
29	chr3:109645423-109645473	K562	blood:	n/a
30	chr3:109735618-109735668	GM12892	blood:	n/a
31	chr3:109735618-109735668	NHDF-neo	bronchial:	n/a
32	chr3:109735618-109735668	HEK293	kidney:	embryo
33	chr3:109735618-109735668	HNPCEpiC	eye:	n/a
34	chr3:109645423-109645473	AG04449	skin:	fetal
35	chr3:109645423-109645473	GM06990	blood:	n/a
36	chr3:109735618-109735668	NH-A	brain:	n/a
37	chr3:109645423-109645473	HAEpiC	amniotic membrane:	n/a
38	chr3:109645423-109645473	ovcar-3	ovarian:	n/a
39	chr3:109645423-109645473	AG09309	skin:	n/a
40	chr3:109645423-109645473	HEK293	kidney:	embryo
41	chr3:109645423-109645473	ECC-1	luminal epithelium:	n/a
42	chr3:109735618-109735668	SAEC	small airway:	n/a
43	chr3:109735618-109735668	Hepatocyte	liver:	n/a
44	chr3:109735618-109735668	RPTEC	kidney:	n/a
45	chr3:109645423-109645473	HCF	heart:	n/a
46	chr3:109645423-109645473	Jurkat	blood:	n/a
47	chr3:109735618-109735668	LNCaP	prostate:	n/a
48	chr3:109735618-109735668	K562	blood:	n/a
49	chr3:109735618-109735668	PFSK-1	brain:	n/a
50	chr3:109645423-109645473	GM12891	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:109359534..109361675-chr3:109706245..109708957,2	MCF-7	breast:
2	chr3:109682867..109683387-chr5:36941291..36942072,2	MCF-7	breast:
3	chr3:109762400..109764463-chr3:109767701..109770522,2	K562	blood:
4	chr3:109581529..109584501-chr3:109598932..109601248,2	K562	blood:
5	chr12:58935829..58938056-chr3:109671221..109673388,2	MCF-7	breast:
6	chr3:109749391..109751192-chr3:110500927..110502696,2	K562	blood:
7	chr3:109581529..109584501-chr3:109598932..109601248,2	K562	blood:
8	chr3:109641317..109642258-chr6:152662604..152663366,2	MCF-7	breast:
9	chr3:109762400..109764463-chr3:109767701..109770522,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPPA4-3	chr3:109696387-109696614	NONHSAT091128
2	lnc-TRAT1-12	chr3:109589133-109590818	ncRnaDb_ncrna_FR244682_1

No data

Variant related genes	Relation type
ENSG00000214380	TF binding region
ENSG00000243945	TF binding region
ENSG00000214380	CpG island
ENSG00000243945	CpG island
ENSG00000258231	chromatin interactions

Extended variants
information (count: 3036 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3036 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563719082	chr3:109582800-109582801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532642758	chr3:109582854-109582855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573644713	chr3:109582884-109582885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189112759	chr3:109582904-109582905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7649120	chr3:109582957-109582958	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs528647290	chr3:109582972-109582973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548777399	chr3:109583060-109583061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568641894	chr3:109583134-109583135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34135999	chr3:109583203-109583204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs578181453	chr3:109583212-109583213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181494610	chr3:109583234-109583235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377035852	chr3:109583288-109583289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570075897	chr3:109583290-109583291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185647238	chr3:109583310-109583311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562300897	chr3:109583315-109583316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552622514	chr3:109583337-109583338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560597106	chr3:109583354-109583355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190553625	chr3:109583356-109583357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535277738	chr3:109583385-109583386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181023449	chr3:109583435-109583436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575444415	chr3:109583442-109583443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146700199	chr3:109583453-109583454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564381909	chr3:109583525-109583526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73851038	chr3:109583532-109583533	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186053872	chr3:109583558-109583559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs59563885	chr3:109583605-109583606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528618665	chr3:109583632-109583633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542290361	chr3:109583642-109583643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564825419	chr3:109583680-109583681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548496665	chr3:109583703-109583704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73851039	chr3:109583722-109583723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527982669	chr3:109583738-109583739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs603474	chr3:109583769-109583770	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs550818415	chr3:109583781-109583782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139157226	chr3:109583806-109583807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539013343	chr3:109583817-109583818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546610568	chr3:109583846-109583847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368363038	chr3:109583850-109583851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190304035	chr3:109583862-109583863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535582333	chr3:109583905-109583906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373319854	chr3:109583914-109583915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567313978	chr3:109583923-109583924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150931041	chr3:109583960-109583961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545534503	chr3:109583963-109583964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558053845	chr3:109583987-109583988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116797490	chr3:109584004-109584005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34199799	chr3:109584007-109584008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140903428	chr3:109584021-109584022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553357807	chr3:109584063-109584064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573249840	chr3:109584086-109584087	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:109582800-109583200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:109583000-109583800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:109583000-109583800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:109583200-109584000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr3:109583200-109584000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr3:109583200-109584200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr3:109583800-109584400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr3:109584200-109584400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:109588000-109589000	Enhancers	Fetal Brain Male	brain
10	chr3:109588600-109589200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:109593600-109594400	Enhancers	HMEC	breast
12	chr3:109594000-109594400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:109594000-109594400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:109594200-109594600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr3:109595200-109595800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:109618600-109619600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:109618600-109620800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr3:109618600-109621200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr3:109618600-109621200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr3:109618600-109621800	Enhancers	Dnd41	blood
21	chr3:109618800-109619400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:109618800-109619400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr3:109618800-109619600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:109618800-109619600	Enhancers	Small Intestine	intestine
25	chr3:109618800-109620400	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr3:109618800-109620400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr3:109618800-109620400	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr3:109619000-109620000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:109619000-109620000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr3:109619000-109620000	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr3:109619000-109620000	Enhancers	Duodenum Mucosa	Duodenum
32	chr3:109619000-109620400	Enhancers	Hela-S3	cervix
33	chr3:109619000-109621000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr3:109619000-109621200	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr3:109619200-109620000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr3:109619400-109620000	Enhancers	Fetal Intestine Large	intestine
37	chr3:109619600-109620400	Enhancers	Stomach Mucosa	stomach
38	chr3:109619800-109621200	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr3:109620000-109621200	Weak transcription	Fetal Intestine Large	intestine
40	chr3:109621200-109621400	Enhancers	Fetal Intestine Large	intestine
41	chr3:109621200-109621400	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr3:109621200-109621400	Enhancers	Small Intestine	intestine
43	chr3:109621200-109622200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr3:109622200-109622400	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr3:109622200-109622400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr3:109624000-109625000	ZNF genes & repeats	Dnd41	blood
47	chr3:109624400-109625000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr3:109629000-109630600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:109629600-109630000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:109630000-109642400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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