Variant report

Variant	esv3389683
Chromosome Location	chr2:233749588-233750923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:490)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:233750681-233751053	GM12878	blood:	n/a	n/a
2	BCL3	chr2:233750738-233751106	GM12878	blood:	n/a	n/a
3	CTCF	chr2:233749620-233749770	GM12866	blood:	n/a	n/a
4	CTCF	chr2:233750854-233751105	GM19239	blood:	n/a	n/a
5	FOSL2	chr2:233748515-233749918	HepG2	liver:	n/a	n/a
6	MYC	chr2:233750914-233751016	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr2:233749617-233749876	ECC-1	luminal epithelium:	n/a	n/a
8	POLR2A	chr2:233750294-233750500	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr2:233749627-233750069	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr2:233746949-233749890	HepG2	liver:	n/a	n/a
11	POLR2A	chr2:233750649-233751166	HepG2	liver:	n/a	n/a
12	POLR2A	chr2:233746770-233751258	HepG2	liver:	n/a	n/a
13	POLR2A	chr2:233749914-233749927	HepG2	liver:	n/a	n/a
14	POLR2A	chr2:233750272-233750278	A549	lung:	n/a	n/a
15	POLR2A	chr2:233749673-233749727	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr2:233748450-233750034	A549	lung:	n/a	n/a
17	POLR2A	chr2:233749667-233749774	A549	lung:	n/a	n/a
18	POLR2A	chr2:233750729-233751078	HCT-116	colon:	n/a	n/a
19	POLR2A	chr2:233750755-233751183	HepG2	liver:	n/a	n/a
20	POLR2A	chr2:233750533-233751391	HepG2	liver:	n/a	n/a
21	POLR2A	chr2:233746538-233749849	HepG2	liver:	n/a	n/a
22	POLR2A	chr2:233750518-233750530	HepG2	liver:	n/a	n/a
23	POLR2A	chr2:233750846-233751144	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr2:233737594-233750472	HepG2	liver:	n/a	n/a
25	SUZ12	chr2:233750716-233751190	H1-hESC	embryonic stem cell:	n/a	n/a
26	TCF12	chr2:233750681-233751166	HepG2	liver:	n/a	n/a
27	USF2	chr2:233750631-233750951	HepG2	liver:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:233750457-233750507	GM12892	blood:	n/a
2	chr2:233749749-233749799	BJ	skin:	n/a
3	chr2:233750457-233750507	GM12892	blood:	n/a
4	chr2:233749749-233749799	BJ	skin:	n/a
5	chr2:233750589-233750639	SK-N-SH_RA	brain:	n/a
6	chr2:233750055-233750105	NHBE	bronchial:	n/a
7	chr2:233749913-233749963	GM12891	blood:	n/a
8	chr2:233749813-233749863	MCF10A-Er-Src	breast:	n/a
9	chr2:233750541-233750591	Hepatocyte	liver:	n/a
10	chr2:233750457-233750507	AG09319	gingival:	n/a
11	chr2:233749813-233749863	HUVEC	blood vessel:	n/a
12	chr2:233749913-233749963	GM19239	blood:	n/a
13	chr2:233749813-233749863	MCF-7	breast:	n/a
14	chr2:233749749-233749799	LNCaP	prostate:	n/a
15	chr2:233749736-233749786	GM12892	blood:	n/a
16	chr2:233750589-233750639	HMEC	breast:	n/a
17	chr2:233750457-233750507	PFSK-1	brain:	n/a
18	chr2:233749913-233749963	NHBE	bronchial:	n/a
19	chr2:233750055-233750105	A549	lung:	n/a
20	chr2:233749736-233749786	AG04449	skin:	fetal
21	chr2:233750457-233750507	HCT-116	colon:	n/a
22	chr2:233750541-233750591	ovcar-3	ovarian:	n/a
23	chr2:233750457-233750507	AG10803	skin:	n/a
24	chr2:233749813-233749863	NB4	blood:	n/a
25	chr2:233749736-233749786	HAEpiC	amniotic membrane:	n/a
26	chr2:233750541-233750591	MCF10A-Er-Src	breast:	n/a
27	chr2:233750457-233750507	GM12891	blood:	n/a
28	chr2:233750055-233750105	BJ	skin:	n/a
29	chr2:233749813-233749863	HEK293	kidney:	embryo
30	chr2:233750541-233750591	HEEpiC	esophagus:	n/a
31	chr2:233749813-233749863	Hela-S3	cervix:	n/a
32	chr2:233750589-233750639	NH-A	brain:	n/a
33	chr2:233749913-233749963	HMEC	breast:	n/a
34	chr2:233749736-233749786	NHBE	bronchial:	n/a
35	chr2:233749749-233749799	T-47D	breast:	n/a
36	chr2:233750457-233750507	T-47D	breast:	n/a
37	chr2:233749913-233749963	Caco-2	colon:	n/a
38	chr2:233750541-233750591	ProgFib	skin:	n/a
39	chr2:233749736-233749786	HCF	heart:	n/a
40	chr2:233749749-233749799	BE2_C	brain:	n/a
41	chr2:233750457-233750507	HepG2	liver:	n/a
42	chr2:233749813-233749863	IMR90	lung:	fetal
43	chr2:233749736-233749786	SK-N-SH	brain:	n/a
44	chr2:233749749-233749799	NH-A	brain:	n/a
45	chr2:233750055-233750105	HIPEpiC	eye:	n/a
46	chr2:233749813-233749863	AG04449	skin:	fetal
47	chr2:233750589-233750639	Caco-2	colon:	n/a
48	chr2:233749736-233749786	HCT-116	colon:	n/a
49	chr2:233750055-233750105	HNPCEpiC	eye:	n/a
50	chr2:233750457-233750507	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:233748378..233751543-chr2:233754163..233756692,4	MCF-7	breast:
2	chr2:233739591..233745527-chr2:233747956..233752237,8	MCF-7	breast:
3	chr2:233749631..233751772-chr2:234261254..234263295,2	MCF-7	breast:

No data

Variant related genes	Relation type
NGEF	TF binding region
NGEF	CpG island
ENSG00000077044	chromatin interactions
ENSG00000243637	chromatin interactions
ENSG00000182600	chromatin interactions
ENSG00000259793	chromatin interactions
ENSG00000066248	chromatin interactions

Extended variants
information (count: 95 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566056569	chr2:233749606-233749607	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs75460861	chr2:233749611-233749612	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs558247473	chr2:233749626-233749627	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs578000549	chr2:233749674-233749675	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs2292724	chr2:233749678-233749679	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374978272	chr2:233749702-233749703	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs368034854	chr2:233749715-233749716	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs532362410	chr2:233749717-233749718	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs112944622	chr2:233749723-233749724	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs542894789	chr2:233749764-233749765	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs534022410	chr2:233749768-233749769	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs189785891	chr2:233749784-233749785	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs374040164	chr2:233749798-233749799	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs564209173	chr2:233749807-233749808	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs572706830	chr2:233749854-233749855	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs549986405	chr2:233749868-233749869	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs368210261	chr2:233749913-233749914	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs80050391	chr2:233749914-233749915	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs549283046	chr2:233749915-233749916	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs554284586	chr2:233749916-233749917	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs373960079	chr2:233749936-233749937	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs551445741	chr2:233749955-233749956	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs372454162	chr2:233749975-233749976	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs571754378	chr2:233749982-233749983	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs376666342	chr2:233749983-233749984	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs112706110	chr2:233749989-233749990	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs369986799	chr2:233750027-233750028	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs149464057	chr2:233750045-233750046	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs144108657	chr2:233750055-233750056	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs557562280	chr2:233750056-233750057	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs2292725	chr2:233750074-233750075	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs182302282	chr2:233750077-233750078	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs139775128	chr2:233750094-233750095	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs2292726	chr2:233750118-233750119	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs368941020	chr2:233750126-233750127	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs541027574	chr2:233750127-233750128	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs372706786	chr2:233750129-233750130	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs557457830	chr2:233750141-233750142	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs577712576	chr2:233750145-233750146	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs144533037	chr2:233750223-233750224	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs563507898	chr2:233750245-233750246	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs529361451	chr2:233750253-233750254	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs185368637	chr2:233750272-233750273	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs113046064	chr2:233750281-233750282	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs549173970	chr2:233750297-233750298	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs542815025	chr2:233750327-233750328	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs191601259	chr2:233750346-233750347	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs528386615	chr2:233750347-233750348	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs146597502	chr2:233750375-233750376	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs565692360	chr2:233750378-233750379	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Hepatocellular carcinoma	22267523	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233726800-233755600	Weak transcription	HSMMtube	muscle
2	chr2:233741600-233749600	Weak transcription	Pancreas	Pancrea
3	chr2:233741800-233750000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr2:233742200-233749800	Weak transcription	Brain Germinal Matrix	brain
5	chr2:233742200-233750000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:233742200-233750800	Weak transcription	Fetal Brain Male	brain
7	chr2:233742400-233752400	Weak transcription	Colonic Mucosa	Colon
8	chr2:233742400-233754200	Strong transcription	Fetal Intestine Small	intestine
9	chr2:233742400-233755600	Weak transcription	Fetal Intestine Large	intestine
10	chr2:233742600-233753400	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr2:233742800-233755600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr2:233743000-233753000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:233743000-233755800	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:233743200-233759600	Strong transcription	Duodenum Mucosa	Duodenum
15	chr2:233744600-233755400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr2:233745200-233753000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr2:233745200-233755600	Weak transcription	Brain Angular Gyrus	brain
18	chr2:233745200-233755800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:233745600-233759800	Strong transcription	Liver	Liver
20	chr2:233746000-233753200	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr2:233746200-233749800	Strong transcription	HepG2	liver
22	chr2:233746200-233753000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr2:233747800-233750800	Weak transcription	Fetal Brain Female	brain
24	chr2:233748400-233750800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:233748400-233750800	Weak transcription	Gastric	stomach
26	chr2:233748600-233751000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:233748800-233749600	ZNF genes & repeats	Esophagus	oesophagus
28	chr2:233748800-233751000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr2:233749000-233749800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:233749000-233752800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:233749200-233749600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:233749200-233749600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr2:233749200-233750000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr2:233749200-233753000	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr2:233749200-233755600	Weak transcription	NHLF	lung
36	chr2:233749400-233751600	Weak transcription	Brain Anterior Caudate	brain
37	chr2:233749400-233766000	Weak transcription	A549	lung
38	chr2:233749600-233749800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:233749600-233749800	Weak transcription	Esophagus	oesophagus
40	chr2:233749600-233751200	Strong transcription	Pancreas	Pancrea
41	chr2:233749800-233750000	Strong transcription	Brain Germinal Matrix	brain
42	chr2:233749800-233750600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:233749800-233750600	Enhancers	Esophagus	oesophagus
44	chr2:233749800-233750600	Weak transcription	HepG2	liver
45	chr2:233749800-233753400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:233750000-233750400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:233750000-233750600	Enhancers	Placenta	Placenta
48	chr2:233750000-233751000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr2:233750000-233755600	Weak transcription	Brain Germinal Matrix	brain
50	chr2:233750200-233750800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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