Variant report

Variant	esv3375822
Chromosome Location	chr2:233750908-233755306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:233750738-233751106	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	chr2:233752851-233753087	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:233753918-233754114	K562	blood:	n/a	chr2:233754022-233754031 chr2:233754022-233754031
6	BHLHE40	chr2:233753008-233753198	K562	blood:	n/a	n/a
7	CHD2	chr2:233751980-233751982	HepG2	liver:	n/a	n/a
8	CHD2	chr2:233753157-233753237	HepG2	liver:	n/a	n/a
9	CTCF	chr2:233752020-233752170	HEK293	kidney:	n/a	n/a
10	CTCF	chr2:233752000-233752150	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr2:233751900-233752050	GM12866	blood:	n/a	n/a
12	CTCF	chr2:233752020-233752170	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr2:233752000-233752150	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr2:233752024-233752101	MCF-7	breast:	n/a	n/a
15	CTCF	chr2:233751980-233752130	HVMF	connective:	n/a	n/a
16	CTCF	chr2:233751980-233752130	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr2:233752000-233752150	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr2:233752038-233752102	MCF-7	breast:	n/a	n/a
19	CTCF	chr2:233752000-233752150	Caco-2	colon:	n/a	n/a
20	CTCF	chr2:233752040-233752190	GM12878	blood:	n/a	n/a
21	CTCF	chr2:233751993-233752136	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr2:233751960-233752110	HepG2	liver:	n/a	n/a
23	CTCF	chr2:233751998-233752118	K562	blood:	n/a	n/a
24	CTCF	chr2:233752013-233752103	GM19239	blood:	n/a	n/a
25	CTCF	chr2:233752006-233752102	MCF-7	breast:	n/a	n/a
26	CTCF	chr2:233752020-233752170	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr2:233752000-233752150	AG09319	gingival:	n/a	n/a
28	CTCF	chr2:233751980-233752130	HRE	kidney:	n/a	n/a
29	CTCF	chr2:233751900-233752050	GM12871	blood:	n/a	n/a
30	CTCF	chr2:233751996-233752101	GM10248	blood:	n/a	n/a
31	CTCF	chr2:233751967-233752157	GM12891	blood:	n/a	n/a
32	CTCF	chr2:233751932-233752155	A549	lung:	n/a	n/a
33	CTCF	chr2:233751920-233752070	A549	lung:	n/a	n/a
34	CTCF	chr2:233751980-233752130	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr2:233751980-233752130	HFF	foreskin:	n/a	n/a
36	CTCF	chr2:233751904-233752182	A549	lung:	n/a	n/a
37	CTCF	chr2:233752020-233752170	NHEK	skin:	n/a	n/a
38	CTCF	chr2:233752000-233752150	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr2:233752003-233752125	GM12878	blood:	n/a	n/a
40	CTCF	chr2:233751940-233752090	GM12869	blood:	n/a	n/a
41	CTCF	chr2:233750854-233751105	GM19239	blood:	n/a	n/a
42	CTCF	chr2:233752000-233752150	GM06990	blood:	n/a	n/a
43	CTCF	chr2:233752937-233753094	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:233752000-233752150	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr2:233751920-233752070	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr2:233751940-233752090	GM12864	blood:	n/a	n/a
47	CTCF	chr2:233751960-233752110	HMF	breast:	n/a	n/a
48	CTCF	chr2:233752000-233752150	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr2:233751940-233752090	HMEC	breast:	n/a	n/a
50	CTCF	chr2:233751980-233752130	NHDF-neo	bronchial:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr2:233748622..233750691-chr2:233751961..233754104,3	K562	blood:
2	chr2:233748378..233751543-chr2:233754163..233756692,4	MCF-7	breast:
3	chr2:233749631..233751772-chr2:234261254..234263295,2	MCF-7	breast:
4	chr2:233746909..233748527-chr2:233752427..233754026,2	MCF-7	breast:
5	chr2:233746656..233750390-chr2:233751961..233755416,5	K562	blood:
6	chr2:233739591..233745527-chr2:233747956..233752237,8	MCF-7	breast:
7	chr2:233739669..233741368-chr2:233754744..233756796,2	MCF-7	breast:
8	chr2:233748378..233751543-chr2:233754163..233756692,4	MCF-7	breast:

No data

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

Extended variants
information (count: 258 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:258 , 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	rs369544162	chr2:233750923-233750924	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs569504867	chr2:233750964-233750965	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs6706932	chr2:233750971-233750972	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556987225	chr2:233750984-233750985	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs10454739	chr2:233751007-233751008	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs547045092	chr2:233751020-233751021	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs188031606	chr2:233751027-233751028	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs116934712	chr2:233751076-233751077	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs572970806	chr2:233751077-233751078	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs373219169	chr2:233751092-233751093	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs545162354	chr2:233751105-233751106	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs565039636	chr2:233751106-233751107	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs575458841	chr2:233751120-233751121	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs191343589	chr2:233751122-233751123	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs560941559	chr2:233751129-233751130	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs183966295	chr2:233751149-233751150	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs375850418	chr2:233751150-233751151	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs546672234	chr2:233751183-233751184	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs560599950	chr2:233751193-233751194	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs115604119	chr2:233751195-233751196	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs552691555	chr2:233751199-233751200	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs188646615	chr2:233751210-233751211	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs538529318	chr2:233751211-233751212	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs114663810	chr2:233751231-233751232	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs536201823	chr2:233751238-233751239	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs536221831	chr2:233751246-233751247	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs6736310	chr2:233751261-233751262	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572851359	chr2:233751285-233751286	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs538466916	chr2:233751309-233751310	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs202163459	chr2:233751327-233751328	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs55796689	chr2:233751333-233751334	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs114722246	chr2:233751334-233751335	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs544077941	chr2:233751335-233751336	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs398091162	chr2:233751342-233751343	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs201962668	chr2:233751343-233751344	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs2592126	chr2:233751377-233751378	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs192935365	chr2:233751401-233751402	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs540205587	chr2:233751433-233751434	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs556146106	chr2:233751471-233751472	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs369612855	chr2:233751480-233751481	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs532598244	chr2:233751502-233751503	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs552541772	chr2:233751582-233751583	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs563076149	chr2:233751601-233751602	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs543452587	chr2:233751612-233751613	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs532080061	chr2:233751622-233751623	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs112149281	chr2:233751633-233751634	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs529394907	chr2:233751640-233751641	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs542728525	chr2:233751730-233751731	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs568744000	chr2:233751731-233751732	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs184993362	chr2:233751737-233751738	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 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:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233726800-233755600	Weak transcription	HSMMtube	muscle
2	chr2:233742400-233752400	Weak transcription	Colonic Mucosa	Colon
3	chr2:233742400-233754200	Strong transcription	Fetal Intestine Small	intestine
4	chr2:233742400-233755600	Weak transcription	Fetal Intestine Large	intestine
5	chr2:233742600-233753400	Strong transcription	Rectal Mucosa Donor 29	rectum
6	chr2:233742800-233755600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr2:233743000-233753000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:233743000-233755800	Weak transcription	Brain Hippocampus Middle	brain
9	chr2:233743200-233759600	Strong transcription	Duodenum Mucosa	Duodenum
10	chr2:233744600-233755400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:233745200-233753000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr2:233745200-233755600	Weak transcription	Brain Angular Gyrus	brain
13	chr2:233745200-233755800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:233745600-233759800	Strong transcription	Liver	Liver
15	chr2:233746000-233753200	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr2:233746200-233753000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr2:233748600-233751000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:233748800-233751000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:233749000-233752800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr2:233749200-233753000	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr2:233749200-233755600	Weak transcription	NHLF	lung
22	chr2:233749400-233751600	Weak transcription	Brain Anterior Caudate	brain
23	chr2:233749400-233766000	Weak transcription	A549	lung
24	chr2:233749600-233751200	Strong transcription	Pancreas	Pancrea
25	chr2:233749800-233753400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:233750000-233751000	Enhancers	Placenta Amnion	Placenta Amnion
27	chr2:233750000-233755600	Weak transcription	Brain Germinal Matrix	brain
28	chr2:233750200-233751000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:233750600-233751200	Genic enhancers	Esophagus	oesophagus
30	chr2:233750600-233755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:233750600-233759800	Strong transcription	HepG2	liver
32	chr2:233750800-233751000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:233750800-233751000	ZNF genes & repeats	Fetal Kidney	kidney
34	chr2:233750800-233751200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:233750800-233751200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:233750800-233751200	ZNF genes & repeats	Fetal Brain Male	brain
37	chr2:233750800-233751200	Strong transcription	Fetal Brain Female	brain
38	chr2:233750800-233751200	Bivalent/Poised TSS	Fetal Lung	lung
39	chr2:233750800-233751200	ZNF genes & repeats	Gastric	stomach
40	chr2:233750800-233761000	Weak transcription	Stomach Mucosa	stomach
41	chr2:233751000-233751200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:233751000-233751200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:233751000-233753000	Weak transcription	Fetal Kidney	kidney
44	chr2:233751000-233755600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr2:233751000-233766000	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr2:233751200-233752800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:233751200-233752800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:233751200-233752800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:233751200-233753400	Strong transcription	Esophagus	oesophagus
50	chr2:233751200-233755400	Weak transcription	Pancreas	Pancrea

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