Variant report

Variant	esv3398860
Chromosome Location	chr2:233747791-233753092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:794)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 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	chr2:233750681-233751053	GM12878	blood:	n/a	n/a
4	BCL3	chr2:233750738-233751106	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	chr2:233751017-233751094	NHEK	skin:	n/a	n/a
10	CTCF	chr2:233751831-233752201	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr2:233751960-233752110	SAEC	small airway:	n/a	n/a
12	CTCF	chr2:233751900-233752050	K562	blood:	n/a	n/a
13	CTCF	chr2:233751906-233752216	K562	blood:	n/a	n/a
14	CTCF	chr2:233751998-233752118	K562	blood:	n/a	n/a
15	CTCF	chr2:233752000-233752150	GM06990	blood:	n/a	n/a
16	CTCF	chr2:233751960-233752110	HepG2	liver:	n/a	n/a
17	CTCF	chr2:233752937-233753094	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr2:233751980-233752130	GM12864	blood:	n/a	n/a
19	CTCF	chr2:233752000-233752150	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr2:233752000-233752150	BE2_C	brain:	n/a	n/a
21	CTCF	chr2:233751960-233752110	GM12874	blood:	n/a	n/a
22	CTCF	chr2:233748906-233748937	LNCaP	prostate:	n/a	n/a
23	CTCF	chr2:233751900-233752050	GM12871	blood:	n/a	n/a
24	CTCF	chr2:233751993-233752153	GM19238	blood:	n/a	n/a
25	CTCF	chr2:233751972-233752141	GM19240	blood:	n/a	n/a
26	CTCF	chr2:233751960-233752110	AG10803	skin:	n/a	n/a
27	CTCF	chr2:233751980-233752130	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr2:233752000-233752150	AG04450	lung:	n/a	n/a
29	CTCF	chr2:233751980-233752130	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr2:233752000-233752150	Caco-2	colon:	n/a	n/a
31	CTCF	chr2:233751900-233752050	GM12866	blood:	n/a	n/a
32	CTCF	chr2:233751940-233752090	GM12864	blood:	n/a	n/a
33	CTCF	chr2:233752000-233752150	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr2:233752931-233753248	GM19239	blood:	n/a	n/a
35	CTCF	chr2:233751977-233752146	A549	lung:	n/a	n/a
36	CTCF	chr2:233751820-233751970	GM12872	blood:	n/a	n/a
37	CTCF	chr2:233751960-233752110	HRE	kidney:	n/a	n/a
38	CTCF	chr2:233752040-233752190	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr2:233751980-233752130	HAc	cerebellar:	n/a	n/a
40	CTCF	chr2:233752024-233752101	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:233751900-233752050	RPTEC	kidney:	n/a	n/a
42	CTCF	chr2:233751996-233752101	GM10248	blood:	n/a	n/a
43	CTCF	chr2:233751980-233752130	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr2:233751980-233752130	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr2:233751780-233752323	A549	lung:	n/a	n/a
46	CTCF	chr2:233751966-233752159	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr2:233751960-233752110	AG09309	skin:	n/a	n/a
48	CTCF	chr2:233751945-233752172	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr2:233752074-233752099	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr2:233752000-233752150	HCPEpiC	choroid plexus:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:233750541-233750591	HAEpiC	amniotic membrane:	n/a
2	chr2:233750541-233750591	HAEpiC	amniotic membrane:	n/a
3	chr2:233750055-233750105	NHBE	bronchial:	n/a
4	chr2:233749813-233749863	NHDF-neo	bronchial:	n/a
5	chr2:233749736-233749786	T-47D	breast:	n/a
6	chr2:233747903-233747953	Hepatocyte	liver:	n/a
7	chr2:233749736-233749786	HNPCEpiC	eye:	n/a
8	chr2:233749442-233749492	PrEC	prostate:	n/a
9	chr2:233750457-233750507	GM19239	blood:	n/a
10	chr2:233749413-233749463	Caco-2	colon:	n/a
11	chr2:233749913-233749963	AG10803	skin:	n/a
12	chr2:233749813-233749863	HAEpiC	amniotic membrane:	n/a
13	chr2:233749813-233749863	HL-60	blood:	n/a
14	chr2:233750457-233750507	AG09319	gingival:	n/a
15	chr2:233750457-233750507	NB4	blood:	n/a
16	chr2:233748276-233748326	ovcar-3	ovarian:	n/a
17	chr2:233750055-233750105	HL-60	blood:	n/a
18	chr2:233750457-233750507	Hepatocyte	liver:	n/a
19	chr2:233750457-233750507	T-47D	breast:	n/a
20	chr2:233747903-233747953	GM19239	blood:	n/a
21	chr2:233749749-233749799	H1-hESC	embryonic stem cell:	embryo
22	chr2:233750055-233750105	HUVEC	blood vessel:	n/a
23	chr2:233750541-233750591	Jurkat	blood:	n/a
24	chr2:233748146-233748196	Hepatocyte	liver:	n/a
25	chr2:233750589-233750639	ProgFib	skin:	n/a
26	chr2:233749413-233749463	GM12878	blood:	n/a
27	chr2:233749413-233749463	SK-N-MC	brain:	n/a
28	chr2:233749913-233749963	HCPEpiC	choroid plexus:	n/a
29	chr2:233750457-233750507	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:233749749-233749799	HRE	kidney:	n/a
31	chr2:233749736-233749786	HEEpiC	esophagus:	n/a
32	chr2:233750055-233750105	U87	brain:	n/a
33	chr2:233748146-233748196	HUVEC	blood vessel:	n/a
34	chr2:233749913-233749963	SK-N-MC	brain:	n/a
35	chr2:233748146-233748196	HCPEpiC	choroid plexus:	n/a
36	chr2:233749813-233749863	RPTEC	kidney:	n/a
37	chr2:233748276-233748326	Caco-2	colon:	n/a
38	chr2:233749736-233749786	SAEC	small airway:	n/a
39	chr2:233747903-233747953	T-47D	breast:	n/a
40	chr2:233750055-233750105	IMR90	lung:	fetal
41	chr2:233749813-233749863	SK-N-MC	brain:	n/a
42	chr2:233749442-233749492	SAEC	small airway:	n/a
43	chr2:233749813-233749863	HIPEpiC	eye:	n/a
44	chr2:233748276-233748326	HCF	heart:	n/a
45	chr2:233749813-233749863	K562	blood:	n/a
46	chr2:233749913-233749963	HCT-116	colon:	n/a
47	chr2:233749413-233749463	HRCEpiC	kidney:	n/a
48	chr2:233749442-233749492	HAEpiC	amniotic membrane:	n/a
49	chr2:233749813-233749863	U87	brain:	n/a
50	chr2:233750589-233750639	AG09319	gingival:	n/a

(count:8 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 344 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:344 , 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	rs533043197	chr2:233747791-233747792	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139306005	chr2:233747792-233747793	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369896727	chr2:233747803-233747804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11885029	chr2:233747807-233747808	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs537646663	chr2:233747808-233747809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375105542	chr2:233747810-233747811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554707982	chr2:233747843-233747844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372528715	chr2:233747848-233747849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547811140	chr2:233747851-233747852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146125316	chr2:233747852-233747853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540131734	chr2:233747863-233747864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35684440	chr2:233747868-233747869	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs373437073	chr2:233747872-233747873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184107493	chr2:233747880-233747881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138962846	chr2:233747898-233747899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562845153	chr2:233747901-233747902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531792273	chr2:233747902-233747903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548543516	chr2:233747931-233747932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372671622	chr2:233747985-233747986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562266301	chr2:233747986-233747987	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs377145247	chr2:233747992-233747993	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528022398	chr2:233748000-233748001	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199562149	chr2:233748006-233748007	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571120890	chr2:233748007-233748008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538276030	chr2:233748009-233748010	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60185884	chr2:233748010-233748011	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376108516	chr2:233748029-233748030	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568867702	chr2:233748047-233748048	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs370768595	chr2:233748054-233748055	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs138129440	chr2:233748065-233748066	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374462143	chr2:233748080-233748081	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554390366	chr2:233748093-233748094	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368730371	chr2:233748101-233748102	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113037652	chr2:233748129-233748130	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370324186	chr2:233748146-233748147	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141871026	chr2:233748147-233748148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs61729908	chr2:233748162-233748163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs533705650	chr2:233748201-233748202	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553671728	chr2:233748208-233748209	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576681258	chr2:233748254-233748255	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs75773908	chr2:233748276-233748277	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562893595	chr2:233748317-233748318	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576511045	chr2:233748328-233748329	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569799895	chr2:233748335-233748336	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542290031	chr2:233748360-233748361	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs370657425	chr2:233748366-233748367	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs73999707	chr2:233748412-233748413	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369670252	chr2:233748428-233748429	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs188787634	chr2:233748452-233748453	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs117487551	chr2:233748468-233748469	Weak transcription 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:121 , 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	chr2:233743000-233748000	Weak transcription	Brain Substantia Nigra	brain
14	chr2:233743000-233753000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:233743000-233755800	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:233743200-233759600	Strong transcription	Duodenum Mucosa	Duodenum
17	chr2:233744600-233755400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr2:233745200-233747800	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr2:233745200-233748400	Weak transcription	A549	lung
20	chr2:233745200-233753000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr2:233745200-233755600	Weak transcription	Brain Angular Gyrus	brain
22	chr2:233745200-233755800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr2:233745600-233748800	Strong transcription	Esophagus	oesophagus
24	chr2:233745600-233759800	Strong transcription	Liver	Liver
25	chr2:233746000-233753200	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr2:233746200-233749800	Strong transcription	HepG2	liver
27	chr2:233746200-233753000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:233746600-233747800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:233746600-233748200	Strong transcription	Fetal Stomach	stomach
30	chr2:233746600-233748600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:233746800-233748800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr2:233746800-233749000	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr2:233747000-233747800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:233747000-233748400	Strong transcription	Gastric	stomach
35	chr2:233747000-233748600	Weak transcription	Brain Anterior Caudate	brain
36	chr2:233747400-233747800	Strong transcription	Fetal Brain Female	brain
37	chr2:233747600-233749200	Strong transcription	NHLF	lung
38	chr2:233747800-233748200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:233747800-233748200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:233747800-233749200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr2:233747800-233750800	Weak transcription	Fetal Brain Female	brain
42	chr2:233748200-233748400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:233748200-233748400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:233748200-233749000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:233748400-233749400	Strong transcription	A549	lung
46	chr2:233748400-233750800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:233748400-233750800	Weak transcription	Gastric	stomach
48	chr2:233748600-233748800	Strong transcription	Brain Anterior Caudate	brain
49	chr2:233748600-233751000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:233748800-233749000	Weak transcription	Brain Anterior Caudate	brain

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