Variant report

Variant	esv3341375
Chromosome Location	chr2:233748808-233753106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:610)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:233752851-233753087	GM12878	blood:	n/a	n/a
2	BCL3	chr2:233752756-233753116	GM12878	blood:	n/a	n/a
3	BCL3	chr2:233750738-233751106	GM12878	blood:	n/a	n/a
4	BCL3	chr2:233750681-233751053	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:233749088-233749213	K562	blood:	n/a	n/a
6	BHLHE40	chr2:233753008-233753198	K562	blood:	n/a	n/a
7	CHD2	chr2:233751980-233751982	HepG2	liver:	n/a	n/a
8	CHD2	chr2:233748751-233748977	HepG2	liver:	n/a	n/a
9	CTCF	chr2:233751960-233752110	MCF-7	breast:	n/a	n/a
10	CTCF	chr2:233751993-233752136	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr2:233752000-233752150	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr2:233751980-233752130	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr2:233752006-233752102	MCF-7	breast:	n/a	n/a
14	CTCF	chr2:233752020-233752170	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr2:233751996-233752101	GM10248	blood:	n/a	n/a
16	CTCF	chr2:233751917-233752244	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr2:233752074-233752099	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr2:233751998-233752118	K562	blood:	n/a	n/a
19	CTCF	chr2:233751940-233752090	AG09319	gingival:	n/a	n/a
20	CTCF	chr2:233751900-233752050	GM12866	blood:	n/a	n/a
21	CTCF	chr2:233751900-233752050	GM12871	blood:	n/a	n/a
22	CTCF	chr2:233752020-233752170	HEK293	kidney:	n/a	n/a
23	CTCF	chr2:233751980-233752130	AG09309	skin:	n/a	n/a
24	CTCF	chr2:233752000-233752150	HVMF	connective:	n/a	n/a
25	CTCF	chr2:233751940-233752090	HCFaa	heart:	n/a	n/a
26	CTCF	chr2:233751960-233752110	GM12874	blood:	n/a	n/a
27	CTCF	chr2:233752020-233752170	HCM	heart:	n/a	n/a
28	CTCF	chr2:233751017-233751094	NHEK	skin:	n/a	n/a
29	CTCF	chr2:233751960-233752110	HCT-116	colon:	n/a	n/a
30	CTCF	chr2:233751960-233752110	AG09309	skin:	n/a	n/a
31	CTCF	chr2:233752000-233752150	AG04450	lung:	n/a	n/a
32	CTCF	chr2:233751780-233752323	A549	lung:	n/a	n/a
33	CTCF	chr2:233751972-233752141	GM19240	blood:	n/a	n/a
34	CTCF	chr2:233751940-233752090	GM12869	blood:	n/a	n/a
35	CTCF	chr2:233751975-233752152	NHEK	skin:	n/a	n/a
36	CTCF	chr2:233752000-233752150	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr2:233751940-233752090	HMF	breast:	n/a	n/a
38	CTCF	chr2:233752000-233752150	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr2:233751906-233752216	K562	blood:	n/a	n/a
40	CTCF	chr2:233752937-233753094	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr2:233751980-233752130	AG10803	skin:	n/a	n/a
42	CTCF	chr2:233751980-233752130	HAc	cerebellar:	n/a	n/a
43	CTCF	chr2:233751980-233752130	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr2:233748906-233748937	LNCaP	prostate:	n/a	n/a
45	CTCF	chr2:233751986-233752114	A549	lung:	n/a	n/a
46	CTCF	chr2:233751922-233752141	HepG2	liver:	n/a	n/a
47	CTCF	chr2:233752020-233752170	NHEK	skin:	n/a	n/a
48	CTCF	chr2:233751960-233752110	HepG2	liver:	n/a	n/a
49	CTCF	chr2:233752000-233752150	K562	blood:	n/a	n/a
50	CTCF	chr2:233751982-233752147	GM12892	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:233749913-233749963	GM06990	blood:	n/a
2	chr2:233750055-233750105	IMR90	lung:	fetal
3	chr2:233750055-233750105	AG10803	skin:	n/a
4	chr2:233750055-233750105	GM06990	blood:	n/a
5	chr2:233749736-233749786	Jurkat	blood:	n/a
6	chr2:233749813-233749863	PANC-1	pancreas:	n/a
7	chr2:233749749-233749799	HRCEpiC	kidney:	n/a
8	chr2:233750055-233750105	BJ	skin:	n/a
9	chr2:233749749-233749799	HEK293	kidney:	embryo
10	chr2:233749413-233749463	HRPEpiC	eye:	n/a
11	chr2:233750541-233750591	GM19239	blood:	n/a
12	chr2:233750055-233750105	NH-A	brain:	n/a
13	chr2:233749913-233749963	ECC-1	luminal epithelium:	n/a
14	chr2:233749736-233749786	HCT-116	colon:	n/a
15	chr2:233750541-233750591	SK-N-SH	brain:	n/a
16	chr2:233750541-233750591	HCT-116	colon:	n/a
17	chr2:233749413-233749463	Hepatocyte	liver:	n/a
18	chr2:233749749-233749799	T-47D	breast:	n/a
19	chr2:233749749-233749799	HIPEpiC	eye:	n/a
20	chr2:233749913-233749963	MCF10A-Er-Src	breast:	n/a
21	chr2:233749413-233749463	IMR90	lung:	fetal
22	chr2:233749736-233749786	AG04449	skin:	fetal
23	chr2:233749749-233749799	AG04449	skin:	fetal
24	chr2:233750589-233750639	NT2-D1	testis:	n/a
25	chr2:233749813-233749863	HL-60	blood:	n/a
26	chr2:233749413-233749463	HAEpiC	amniotic membrane:	n/a
27	chr2:233749813-233749863	NHBE	bronchial:	n/a
28	chr2:233749749-233749799	AG10803	skin:	n/a
29	chr2:233749736-233749786	NHDF-neo	bronchial:	n/a
30	chr2:233750457-233750507	HIPEpiC	eye:	n/a
31	chr2:233750589-233750639	HCM	heart:	n/a
32	chr2:233750457-233750507	ECC-1	luminal epithelium:	n/a
33	chr2:233750541-233750591	Jurkat	blood:	n/a
34	chr2:233749913-233749963	HUVEC	blood vessel:	n/a
35	chr2:233749913-233749963	AG04450	lung:	fetal
36	chr2:233750589-233750639	NHDF-neo	bronchial:	n/a
37	chr2:233750589-233750639	PFSK-1	brain:	n/a
38	chr2:233750541-233750591	NHDF-neo	bronchial:	n/a
39	chr2:233749813-233749863	K562	blood:	n/a
40	chr2:233749736-233749786	HMEC	breast:	n/a
41	chr2:233750055-233750105	SK-N-MC	brain:	n/a
42	chr2:233750457-233750507	HUVEC	blood vessel:	n/a
43	chr2:233749913-233749963	GM12878	blood:	n/a
44	chr2:233750541-233750591	MCF-7	breast:	n/a
45	chr2:233749813-233749863	BE2_C	brain:	n/a
46	chr2:233750457-233750507	H1-hESC	embryonic stem cell:	embryo
47	chr2:233749413-233749463	ECC-1	luminal epithelium:	n/a
48	chr2:233749913-233749963	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:233749913-233749963	NHDF-neo	bronchial:	n/a
50	chr2:233749442-233749492	SK-N-SH	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:233746971..233749458-chr2:233835179..233837399,2	K562	blood:
2	chr2:233748622..233750691-chr2:233751961..233754104,3	K562	blood:
3	chr2:233739591..233745527-chr2:233747956..233752237,8	MCF-7	breast:
4	chr2:233748378..233751543-chr2:233754163..233756692,4	MCF-7	breast:
5	chr2:233746909..233748527-chr2:233752427..233754026,2	MCF-7	breast:
6	chr2:233746656..233750390-chr2:233751961..233755416,5	K562	blood:
7	chr2:233749631..233751772-chr2:234261254..234263295,2	MCF-7	breast:

No data

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

Extended variants
information (count: 283 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372210599	chr2:233748809-233748810	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs556313515	chr2:233748852-233748853	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376849642	chr2:233748861-233748862	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201475244	chr2:233748862-233748863	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200595468	chr2:233748872-233748873	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs372496398	chr2:233748887-233748888	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs572523078	chr2:233748894-233748895	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs541650938	chr2:233748905-233748906	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564658783	chr2:233748918-233748919	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs533501134	chr2:233748926-233748927	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544072267	chr2:233748951-233748952	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs557739596	chr2:233748953-233748954	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376543654	chr2:233748962-233748963	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs112663179	chr2:233748964-233748965	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139690877	chr2:233748986-233748987	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547736458	chr2:233748994-233748995	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs149361590	chr2:233749005-233749006	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527377859	chr2:233749014-233749015	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530864292	chr2:233749026-233749027	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs148425185	chr2:233749027-233749028	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547238865	chr2:233749076-233749077	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570605967	chr2:233749077-233749078	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539388526	chr2:233749110-233749111	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs556433655	chr2:233749124-233749125	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569819628	chr2:233749189-233749190	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs541616553	chr2:233749195-233749196	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs535851118	chr2:233749200-233749201	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146389563	chr2:233749210-233749211	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs555755086	chr2:233749294-233749295	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs572611432	chr2:233749296-233749297	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs79685742	chr2:233749310-233749311	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187137976	chr2:233749334-233749335	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs578111744	chr2:233749379-233749380	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs543626714	chr2:233749387-233749388	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs564012114	chr2:233749400-233749401	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs375748900	chr2:233749414-233749415	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541465844	chr2:233749424-233749425	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561345397	chr2:233749440-233749441	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190230325	chr2:233749442-233749443	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs182416299	chr2:233749443-233749444	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs563992933	chr2:233749463-233749464	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574891248	chr2:233749508-233749509	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184979404	chr2:233749510-233749511	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs569940423	chr2:233749562-233749563	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2675953	chr2:233749565-233749566	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs35757088	chr2:233749573-233749574	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs549445482	chr2:233749581-233749582	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566056569	chr2:233749606-233749607	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs75460861	chr2:233749611-233749612	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs558247473	chr2:233749626-233749627	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 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:104 , 50 per page) page: 1 2 3

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	chr2:233742000-233749000	Weak transcription	Small Intestine	intestine
5	chr2:233742200-233749800	Weak transcription	Brain Germinal Matrix	brain
6	chr2:233742200-233750000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:233742200-233750800	Weak transcription	Fetal Brain Male	brain
8	chr2:233742400-233752400	Weak transcription	Colonic Mucosa	Colon
9	chr2:233742400-233754200	Strong transcription	Fetal Intestine Small	intestine
10	chr2:233742400-233755600	Weak transcription	Fetal Intestine Large	intestine
11	chr2:233742600-233753400	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr2:233742800-233755600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr2:233743000-233753000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:233743000-233755800	Weak transcription	Brain Hippocampus Middle	brain
15	chr2:233743200-233759600	Strong transcription	Duodenum Mucosa	Duodenum
16	chr2:233744600-233755400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr2:233745200-233753000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr2:233745200-233755600	Weak transcription	Brain Angular Gyrus	brain
19	chr2:233745200-233755800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr2:233745600-233759800	Strong transcription	Liver	Liver
21	chr2:233746000-233753200	Strong transcription	Rectal Mucosa Donor 31	rectum
22	chr2:233746200-233749800	Strong transcription	HepG2	liver
23	chr2:233746200-233753000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr2:233746800-233749000	Strong transcription	Brain Inferior Temporal Lobe	brain
25	chr2:233747600-233749200	Strong transcription	NHLF	lung
26	chr2:233747800-233749200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr2:233747800-233750800	Weak transcription	Fetal Brain Female	brain
28	chr2:233748200-233749000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:233748400-233749400	Strong transcription	A549	lung
30	chr2:233748400-233750800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr2:233748400-233750800	Weak transcription	Gastric	stomach
32	chr2:233748600-233751000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:233748800-233749000	Weak transcription	Brain Anterior Caudate	brain
34	chr2:233748800-233749600	ZNF genes & repeats	Esophagus	oesophagus
35	chr2:233748800-233751000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:233749000-233749400	Genic enhancers	Brain Anterior Caudate	brain
37	chr2:233749000-233749800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:233749000-233752800	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr2:233749200-233749600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr2:233749200-233749600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr2:233749200-233750000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:233749200-233753000	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr2:233749200-233755600	Weak transcription	NHLF	lung
44	chr2:233749400-233751600	Weak transcription	Brain Anterior Caudate	brain
45	chr2:233749400-233766000	Weak transcription	A549	lung
46	chr2:233749600-233749800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr2:233749600-233749800	Weak transcription	Esophagus	oesophagus
48	chr2:233749600-233751200	Strong transcription	Pancreas	Pancrea
49	chr2:233749800-233750000	Strong transcription	Brain Germinal Matrix	brain
50	chr2:233749800-233750600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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