Variant report

Variant	esv3349659
Chromosome Location	chr2:233762108-233766506
allele	n/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	BATF	chr2:233764531-233764799	GM12878	blood:	n/a	n/a
2	BCL11A	chr2:233765234-233765563	GM12878	blood:	n/a	n/a
3	BCL11A	chr2:233764191-233764835	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:233764992-233765227	GM12878	blood:	n/a	n/a
5	BCL3	chr2:233765229-233765708	GM12878	blood:	n/a	n/a
6	BCL3	chr2:233763417-233765657	GM12878	blood:	n/a	n/a
7	BCL3	chr2:233763418-233764598	GM12878	blood:	n/a	n/a
8	BCL3	chr2:233764696-233765215	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:233766428-233767044	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr2:233766474-233767106	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr2:233763243-233763320	LNCaP	prostate:	n/a	n/a
12	CUX1	chr2:233763256-233763290	K562	blood:	n/a	n/a
13	FOS	chr2:233766288-233767253	HUVEC	blood vessel:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766866-233766877 chr2:233766868-233766875
14	FOSL1	chr2:233766181-233767251	HCT-116	colon:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
15	FOSL1	chr2:233766268-233767381	HCT-116	colon:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
16	FOSL2	chr2:233766258-233767212	SK-N-SH	brain:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
17	FOSL2	chr2:233766391-233767311	A549	lung:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
18	JUN	chr2:233766466-233767184	K562	blood:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
19	JUND	chr2:233766344-233767519	SK-N-SH	brain:	n/a	chr2:233766840-233766851 chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
20	JUND	chr2:233766153-233767346	HCT-116	colon:	n/a	chr2:233766840-233766851 chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
21	JUND	chr2:233766012-233767321	HCT-116	colon:	n/a	chr2:233766840-233766851 chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
22	JUND	chr2:233766499-233767130	SK-N-SH	brain:	n/a	chr2:233766840-233766851 chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
23	MAX	chr2:233766367-233767148	A549	lung:	n/a	n/a
24	MAX	chr2:233766083-233767240	A549	lung:	n/a	n/a
25	MAX	chr2:233762167-233762176	NB4	blood:	n/a	n/a
26	MAX	chr2:233762974-233762995	NB4	blood:	n/a	chr2:233762974-233762984
27	MAX	chr2:233766361-233767028	Hela-S3	cervix:	n/a	n/a
28	MAZ	chr2:233766033-233767102	IMR90	lung:	n/a	n/a
29	MAZ	chr2:233766299-233766999	Hela-S3	cervix:	n/a	n/a
30	MYC	chr2:233762048-233762145	NB4	blood:	n/a	n/a
31	NANOG	chr2:233765636-233765809	H1-hESC	embryonic stem cell:	n/a	chr2:233765718-233765732
32	NFATC1	chr2:233763390-233764109	GM12878	blood:	n/a	n/a
33	NFATC1	chr2:233763564-233764075	GM12878	blood:	n/a	n/a
34	NFATC1	chr2:233764099-233764977	GM12878	blood:	n/a	n/a
35	NFATC1	chr2:233765266-233765646	GM12878	blood:	n/a	n/a
36	NFATC1	chr2:233765214-233765742	GM12878	blood:	n/a	n/a
37	NFIC	chr2:233765134-233765624	GM12878	blood:	n/a	n/a
38	NFIC	chr2:233764160-233764802	GM12878	blood:	n/a	n/a
39	PAX5	chr2:233764224-233765569	GM12878	blood:	n/a	n/a
40	PBX3	chr2:233763459-233763942	GM12878	blood:	n/a	n/a
41	PBX3	chr2:233764064-233765633	GM12878	blood:	n/a	n/a
42	PBX3	chr2:233765352-233765502	GM12878	blood:	n/a	n/a
43	PBX3	chr2:233764459-233764619	GM12878	blood:	n/a	n/a
44	PBX3	chr2:233764892-233765025	GM12878	blood:	n/a	n/a
45	POLR2A	chr2:233763516-233763915	HepG2	liver:	n/a	n/a
46	POLR2A	chr2:233766488-233767045	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr2:233766334-233767185	U87	brain:	n/a	n/a
48	POLR2A	chr2:233762620-233762621	MCF-7	breast:	n/a	n/a
49	POLR2A	chr2:233762624-233762625	MCF-7	breast:	n/a	n/a
50	POLR2A	chr2:233766430-233767019	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:233765616-233765666	HEEpiC	esophagus:	n/a
2	chr2:233765616-233765666	HEEpiC	esophagus:	n/a
3	chr2:233765616-233765666	GM12891	blood:	n/a
4	chr2:233764831-233764881	HEEpiC	esophagus:	n/a
5	chr2:233765872-233765922	PrEC	prostate:	n/a
6	chr2:233766118-233766168	NHBE	bronchial:	n/a
7	chr2:233765616-233765666	PrEC	prostate:	n/a
8	chr2:233762570-233762620	H1-hESC	embryonic stem cell:	embryo
9	chr2:233764831-233764881	HCT-116	colon:	n/a
10	chr2:233766002-233766052	NHDF-neo	bronchial:	n/a
11	chr2:233766002-233766052	H1-hESC	embryonic stem cell:	embryo
12	chr2:233766002-233766052	HUVEC	blood vessel:	n/a
13	chr2:233762570-233762620	GM12891	blood:	n/a
14	chr2:233766002-233766052	HIPEpiC	eye:	n/a
15	chr2:233765872-233765922	GM12891	blood:	n/a
16	chr2:233764831-233764881	PrEC	prostate:	n/a
17	chr2:233766002-233766052	Caco-2	colon:	n/a
18	chr2:233765872-233765922	NB4	blood:	n/a
19	chr2:233766002-233766052	AG09309	skin:	n/a
20	chr2:233765616-233765666	HNPCEpiC	eye:	n/a
21	chr2:233762570-233762620	HRE	kidney:	n/a
22	chr2:233765872-233765922	HCF	heart:	n/a
23	chr2:233765872-233765922	Caco-2	colon:	n/a
24	chr2:233766118-233766168	AG10803	skin:	n/a
25	chr2:233766002-233766052	ProgFib	skin:	n/a
26	chr2:233766118-233766168	CMK	blood:	n/a
27	chr2:233766118-233766168	Hepatocyte	liver:	n/a
28	chr2:233762570-233762620	GM19239	blood:	n/a
29	chr2:233766002-233766052	HCT-116	colon:	n/a
30	chr2:233765872-233765922	SK-N-MC	brain:	n/a
31	chr2:233765872-233765922	T-47D	breast:	n/a
32	chr2:233765616-233765666	HRPEpiC	eye:	n/a
33	chr2:233764831-233764881	AG10803	skin:	n/a
34	chr2:233765616-233765666	HCPEpiC	choroid plexus:	n/a
35	chr2:233766118-233766168	A549	lung:	n/a
36	chr2:233765872-233765922	RPTEC	kidney:	n/a
37	chr2:233762570-233762620	HL-60	blood:	n/a
38	chr2:233765616-233765666	HUVEC	blood vessel:	n/a
39	chr2:233766002-233766052	HRCEpiC	kidney:	n/a
40	chr2:233765872-233765922	GM12878	blood:	n/a
41	chr2:233766002-233766052	CMK	blood:	n/a
42	chr2:233766118-233766168	ProgFib	skin:	n/a
43	chr2:233765872-233765922	NHBE	bronchial:	n/a
44	chr2:233766118-233766168	HNPCEpiC	eye:	n/a
45	chr2:233766002-233766052	GM12891	blood:	n/a
46	chr2:233762570-233762620	AG10803	skin:	n/a
47	chr2:233762570-233762620	SK-N-SH	brain:	n/a
48	chr2:233764831-233764881	ovcar-3	ovarian:	n/a
49	chr2:233764831-233764881	K562	blood:	n/a
50	chr2:233765872-233765922	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:233755071..233758000-chr2:233760102..233763754,5	MCF-7	breast:

Variant related genes	Relation type
NGEF	TF binding region
NGEF	CpG island
ENSG00000066248	chromatin interactions

Extended variants
information (count: 311 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112813227	chr2:233762144-233762145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536013163	chr2:233762168-233762169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs553241345	chr2:233762194-233762195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192380465	chr2:233762195-233762196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545044840	chr2:233762221-233762222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs11885360	chr2:233762225-233762226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575366172	chr2:233762238-233762239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184760616	chr2:233762274-233762275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561199993	chr2:233762310-233762311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530321486	chr2:233762332-233762333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190523332	chr2:233762342-233762343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537971189	chr2:233762351-233762352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560808408	chr2:233762379-233762380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147389247	chr2:233762380-233762381	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139451834	chr2:233762409-233762410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs180883151	chr2:233762440-233762441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530396785	chr2:233762441-233762442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550652219	chr2:233762445-233762446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112522280	chr2:233762454-233762455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs62191781	chr2:233762457-233762458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113779835	chr2:233762498-233762499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs200075425	chr2:233762503-233762504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567209332	chr2:233762571-233762572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145075895	chr2:233762585-233762586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7349454	chr2:233762587-233762588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546472822	chr2:233762610-233762611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs111627129	chr2:233762624-233762625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538528422	chr2:233762627-233762628	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12622812	chr2:233762629-233762630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558398228	chr2:233762631-233762632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75537837	chr2:233762645-233762646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553538300	chr2:233762745-233762746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs77788624	chr2:233762747-233762748	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537806195	chr2:233762768-233762769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200431967	chr2:233762774-233762775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11341358	chr2:233762775-233762776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs71405719	chr2:233762776-233762777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs576732570	chr2:233762782-233762783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs36046872	chr2:233762784-233762785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555058242	chr2:233762793-233762794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574828713	chr2:233762801-233762802	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184515749	chr2:233762826-233762827	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375097152	chr2:233762838-233762839	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560648238	chr2:233762858-233762859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113718721	chr2:233762912-233762913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577648010	chr2:233762947-233762948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546540035	chr2:233763051-233763052	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563128053	chr2:233763052-233763053	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs142231021	chr2:233763054-233763055	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs372948048	chr2:233763062-233763063	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233749400-233766000	Weak transcription	A549	lung
2	chr2:233751000-233766000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:233756200-233763600	Weak transcription	NHLF	lung
4	chr2:233756400-233763800	Weak transcription	Right Atrium	heart
5	chr2:233756600-233763400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:233756600-233766400	Weak transcription	Brain Substantia Nigra	brain
7	chr2:233756800-233765400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:233757000-233765400	Weak transcription	Pancreas	Pancrea
9	chr2:233757000-233766200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:233757000-233766200	Weak transcription	Fetal Brain Female	brain
11	chr2:233757000-233766400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:233757200-233763400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr2:233757400-233776600	Weak transcription	Brain Angular Gyrus	brain
14	chr2:233757600-233763400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr2:233757800-233763400	Weak transcription	Gastric	stomach
16	chr2:233758200-233768800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr2:233759000-233763200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:233759200-233784400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr2:233759400-233763400	Weak transcription	Fetal Intestine Small	intestine
20	chr2:233759400-233765800	Weak transcription	Esophagus	oesophagus
21	chr2:233759600-233762800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr2:233759800-233763200	Weak transcription	Liver	Liver
23	chr2:233759800-233763400	Weak transcription	Spleen	Spleen
24	chr2:233759800-233766000	Weak transcription	Colonic Mucosa	Colon
25	chr2:233759800-233766400	Weak transcription	HepG2	liver
26	chr2:233760600-233762600	Weak transcription	Fetal Brain Male	brain
27	chr2:233761000-233765800	Weak transcription	Brain Anterior Caudate	brain
28	chr2:233761800-233763600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr2:233762800-233764000	Strong transcription	Duodenum Mucosa	Duodenum
30	chr2:233763200-233764000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:233763200-233764200	Strong transcription	Liver	Liver
32	chr2:233763200-233766200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:233763400-233763600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:233763400-233763600	Strong transcription	Fetal Intestine Small	intestine
35	chr2:233763400-233763600	Genic enhancers	Gastric	stomach
36	chr2:233763400-233763600	Enhancers	Stomach Mucosa	stomach
37	chr2:233763400-233764000	Genic enhancers	Brain Cingulate Gyrus	brain
38	chr2:233763400-233764000	Strong transcription	Rectal Mucosa Donor 31	rectum
39	chr2:233763400-233764200	Genic enhancers	Spleen	Spleen
40	chr2:233763600-233763800	Bivalent Enhancer	Fetal Heart	heart
41	chr2:233763600-233763800	Enhancers	Fetal Kidney	kidney
42	chr2:233763600-233763800	Active TSS	Fetal Lung	lung
43	chr2:233763600-233763800	Flanking Active TSS	Right Ventricle	heart
44	chr2:233763600-233764000	Strong transcription	Gastric	stomach
45	chr2:233763600-233764200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr2:233763600-233764200	Enhancers	NHLF	lung
47	chr2:233763600-233764400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:233763600-233765600	Weak transcription	Fetal Intestine Small	intestine
49	chr2:233763600-233766000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:233763800-233764000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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