Variant report

Variant	nsv876015
Chromosome Location	chr2:234518011-234579915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:673)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:234570651-234570703	K562	blood:	n/a	n/a
2	BATF	chr2:234565000-234565385	GM12878	blood:	n/a	n/a
3	BATF	chr2:234565000-234565520	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:234565119-234565303	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:234565052-234565391	GM12878	blood:	n/a	n/a
6	BCL3	chr2:234577236-234577886	A549	lung:	n/a	n/a
7	BCL3	chr2:234579737-234579994	GM12878	blood:	n/a	n/a
8	CEBPB	chr2:234577256-234577747	A549	lung:	n/a	n/a
9	CEBPB	chr2:234521112-234521181	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:234577262-234577872	A549	lung:	n/a	n/a
11	CREB1	chr2:234577380-234577643	A549	lung:	n/a	n/a
12	CTCF	chr2:234551906-234552090	Fibrobl	skin:	n/a	n/a
13	CTCF	chr2:234551920-234552070	MCF-7	breast:	n/a	n/a
14	CTCF	chr2:234551920-234552070	HPF	lung:	n/a	n/a
15	CTCF	chr2:234551904-234552071	HepG2	liver:	n/a	n/a
16	CTCF	chr2:234551980-234552130	HRE	kidney:	n/a	n/a
17	CTCF	chr2:234547580-234547730	GM12864	blood:	n/a	n/a
18	CTCF	chr2:234551940-234552090	GM12864	blood:	n/a	n/a
19	CTCF	chr2:234551920-234552070	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr2:234551900-234552050	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr2:234551620-234551770	GM12868	blood:	n/a	n/a
22	CTCF	chr2:234551940-234552090	GM12878	blood:	n/a	n/a
23	CTCF	chr2:234551910-234552082	GM19238	blood:	n/a	n/a
24	CTCF	chr2:234545228-234545302	NHEK	skin:	n/a	n/a
25	CTCF	chr2:234551900-234552050	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr2:234551900-234552050	GM12875	blood:	n/a	n/a
27	CTCF	chr2:234551746-234552214	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:234551920-234552070	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr2:234547643-234547715	GM19240	blood:	n/a	n/a
30	CTCF	chr2:234551920-234552070	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr2:234551920-234552070	GM12865	blood:	n/a	n/a
32	CTCF	chr2:234551900-234552050	GM12873	blood:	n/a	n/a
33	CTCF	chr2:234547480-234547630	A549	lung:	n/a	n/a
34	CTCF	chr2:234551901-234552076	GM19240	blood:	n/a	n/a
35	CTCF	chr2:234551926-234552069	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr2:234551929-234552062	Gliobla	brain:	n/a	n/a
37	CTCF	chr2:234551900-234552050	NHEK	skin:	n/a	n/a
38	CTCF	chr2:234551860-234552010	GM12865	blood:	n/a	n/a
39	CTCF	chr2:234551890-234552067	GM12878	blood:	n/a	n/a
40	CTCF	chr2:234522915-234522947	GM20000	blood:	n/a	n/a
41	CTCF	chr2:234551868-234552098	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:234551777-234552148	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr2:234552120-234552270	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr2:234551900-234552050	K562	blood:	n/a	n/a
45	CTCF	chr2:234551800-234551950	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr2:234551955-234552034	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr2:234551906-234552081	GM12892	blood:	n/a	n/a
48	CTCF	chr2:234551920-234552070	HMEC	breast:	n/a	n/a
49	CTCF	chr2:234551940-234552090	GM12871	blood:	n/a	n/a
50	CTCF	chr2:234551838-234552159	GM12878	blood:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234525618-234525668	IMR90	lung:	fetal
2	chr2:234526077-234526127	HEK293	kidney:	embryo
3	chr2:234525618-234525668	IMR90	lung:	fetal
4	chr2:234526077-234526127	HEK293	kidney:	embryo
5	chr2:234544995-234545045	AG10803	skin:	n/a
6	chr2:234526255-234526305	CMK	blood:	n/a
7	chr2:234545110-234545160	ProgFib	skin:	n/a
8	chr2:234544271-234544321	HNPCEpiC	eye:	n/a
9	chr2:234525618-234525668	HNPCEpiC	eye:	n/a
10	chr2:234579550-234579600	BE2_C	brain:	n/a
11	chr2:234544462-234544512	GM06990	blood:	n/a
12	chr2:234525618-234525668	LNCaP	prostate:	n/a
13	chr2:234526077-234526127	GM12892	blood:	n/a
14	chr2:234526295-234526345	HAEpiC	amniotic membrane:	n/a
15	chr2:234579873-234579923	HepG2	liver:	n/a
16	chr2:234544462-234544512	ovcar-3	ovarian:	n/a
17	chr2:234526077-234526127	HCT-116	colon:	n/a
18	chr2:234544462-234544512	HCPEpiC	choroid plexus:	n/a
19	chr2:234545110-234545160	HUVEC	blood vessel:	n/a
20	chr2:234526295-234526345	IMR90	lung:	fetal
21	chr2:234526255-234526305	SK-N-SH_RA	brain:	n/a
22	chr2:234544271-234544321	ProgFib	skin:	n/a
23	chr2:234526255-234526305	HAEpiC	amniotic membrane:	n/a
24	chr2:234579550-234579600	AG04450	lung:	fetal
25	chr2:234544271-234544321	K562	blood:	n/a
26	chr2:234526255-234526305	GM19239	blood:	n/a
27	chr2:234526255-234526305	NB4	blood:	n/a
28	chr2:234544995-234545045	AoSMC	blood vessel:	n/a
29	chr2:234544271-234544321	H1-hESC	embryonic stem cell:	embryo
30	chr2:234545110-234545160	HEK293	kidney:	embryo
31	chr2:234526077-234526127	CMK	blood:	n/a
32	chr2:234526295-234526345	AG09319	gingival:	n/a
33	chr2:234545177-234545227	U87	brain:	n/a
34	chr2:234525618-234525668	HCT-116	colon:	n/a
35	chr2:234545177-234545227	AG04450	lung:	fetal
36	chr2:234579550-234579600	PrEC	prostate:	n/a
37	chr2:234544271-234544321	HCT-116	colon:	n/a
38	chr2:234525618-234525668	Hela-S3	cervix:	n/a
39	chr2:234579550-234579600	Jurkat	blood:	n/a
40	chr2:234544462-234544512	HAEpiC	amniotic membrane:	n/a
41	chr2:234544462-234544512	HCT-116	colon:	n/a
42	chr2:234579873-234579923	HIPEpiC	eye:	n/a
43	chr2:234544995-234545045	GM19239	blood:	n/a
44	chr2:234579873-234579923	PFSK-1	brain:	n/a
45	chr2:234579550-234579600	SKMC	muscle:	n/a
46	chr2:234526255-234526305	BE2_C	brain:	n/a
47	chr2:234544462-234544512	U87	brain:	n/a
48	chr2:234579873-234579923	HCT-116	colon:	n/a
49	chr2:234544271-234544321	IMR90	lung:	fetal
50	chr2:234525618-234525668	H1-hESC	embryonic stem cell:	embryo

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	2:234492023-234494396..2:234543708-234558325	GM12878	blood:
2	2:234543708-234558325..2:234772667-234780240	Hela-S3	cervix:
3	chr2:234448748..234450538-chr2:234553700..234555671,2	K562	blood:
4	chr2:234557472..234561426-chr2:234563315..234566249,3	K562	blood:
5	chr2:234577799..234579592-chr2:234583305..234585773,2	K562	blood:
6	chr2:234578802..234581575-chr2:234598668..234600515,2	MCF-7	breast:
7	chr2:234559926..234563165-chr2:234564749..234566368,3	K562	blood:
8	2:234543708-234558325..2:234649753-234657866	Hela-S3	cervix:
9	chr2:234534086..234537809-chr2:234597332..234600775,3	MCF-7	breast:
10	chr2:234559926..234563165-chr2:234564749..234566368,3	K562	blood:
11	chr2:234557472..234561426-chr2:234563315..234566249,3	K562	blood:
12	chr2:234564130..234566542-chr2:234601879..234604853,2	MCF-7	breast:
13	chr2:234544581..234547100-chr2:234548174..234549799,2	MCF-7	breast:

No data

Variant related genes	Relation type
UGT1A13P	TF binding region
UGT1A8	TF binding region
UGT1A10	TF binding region
UGT1A9	TF binding region
UGT1A13P	CpG island
UGT1A8	CpG island
UGT1A10	CpG island
UGT1A9	CpG island
ENSG00000167165	chromatin interactions
ENSG00000228445	chromatin interactions
ENSG00000224287	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000227802	chromatin interactions
ENSG00000228949	chromatin interactions

Extended variants
information (count: 2126 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2126 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2741027	chr2:234518011-234518012	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574620703	chr2:234518030-234518031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540044223	chr2:234518033-234518034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373539556	chr2:234518076-234518077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188681643	chr2:234518080-234518081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546288782	chr2:234518104-234518105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs17863758	chr2:234518109-234518110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562884343	chr2:234518110-234518111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574773201	chr2:234518123-234518124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs80337635	chr2:234518137-234518138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17864667	chr2:234518166-234518167	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs567060258	chr2:234521706-234521707	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs561286013	chr2:234521728-234521729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs539233844	chr2:234521823-234521824	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557928422	chr2:234521862-234521863	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563201298	chr2:234524019-234524020	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs193062305	chr2:234524035-234524036	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs561497636	chr2:234525344-234525345	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs10210058	chr2:234525355-234525356	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs148981671	chr2:234525448-234525449	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs373865399	chr2:234525522-234525523	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs570664217	chr2:234525562-234525563	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183078816	chr2:234525599-234525600	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs550048511	chr2:234525600-234525601	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs367633546	chr2:234525618-234525619	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs570122405	chr2:234525626-234525627	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs45576241	chr2:234525631-234525632	Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs186450852	chr2:234525639-234525640	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs573523307	chr2:234525654-234525655	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs575605726	chr2:234525700-234525701	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs71423605	chr2:234525710-234525711	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs565705061	chr2:234525747-234525748	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs45586436	chr2:234525760-234525761	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs558023639	chr2:234525761-234525762	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577854776	chr2:234525795-234525796	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs543977941	chr2:234525813-234525814	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs4114768	chr2:234525824-234525825	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs113910749	chr2:234525868-234525869	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529035590	chr2:234525876-234525877	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs576107211	chr2:234525893-234525894	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs541526041	chr2:234525978-234525979	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs189645806	chr2:234525986-234525987	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs527937689	chr2:234526035-234526036	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs116655560	chr2:234526046-234526047	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548002226	chr2:234526130-234526131	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148224012	chr2:234526131-234526132	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373737548	chr2:234526150-234526151	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11415286	chr2:234526223-234526224	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78219233	chr2:234526224-234526225	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397988271	chr2:234526237-234526238	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Chronic myeloid leukemia	21384125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234516600-234518200	Enhancers	Liver	Liver
2	chr2:234525600-234528200	Active TSS	Rectal Mucosa Donor 29	rectum
3	chr2:234525800-234526000	Enhancers	Duodenum Mucosa	Duodenum
4	chr2:234525800-234526200	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr2:234525800-234526400	Enhancers	NHEK	skin
6	chr2:234526000-234526600	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr2:234526200-234526600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
8	chr2:234526600-234526800	Enhancers	Duodenum Mucosa	Duodenum
9	chr2:234526600-234526800	Active TSS	Rectal Mucosa Donor 31	rectum
10	chr2:234526800-234528800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr2:234526800-234528800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr2:234528800-234529000	Enhancers	Duodenum Mucosa	Duodenum
13	chr2:234528800-234529600	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr2:234537800-234538000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
15	chr2:234538000-234544600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr2:234544400-234545200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr2:234544600-234544800	Enhancers	Duodenum Mucosa	Duodenum
18	chr2:234544600-234544800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr2:234544600-234545000	Enhancers	Colonic Mucosa	Colon
20	chr2:234544800-234547600	Active TSS	Duodenum Mucosa	Duodenum
21	chr2:234544800-234548400	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr2:234545200-234545600	Active TSS	Rectal Mucosa Donor 31	rectum
23	chr2:234545200-234545800	Active TSS	Colonic Mucosa	Colon
24	chr2:234545200-234546000	Active TSS	Rectal Smooth Muscle	rectum
25	chr2:234545600-234546000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
26	chr2:234545800-234547400	Weak transcription	Colonic Mucosa	Colon
27	chr2:234546000-234546800	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr2:234546800-234547200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr2:234547200-234548000	Active TSS	Rectal Mucosa Donor 31	rectum
30	chr2:234547400-234547800	Active TSS	Colonic Mucosa	Colon
31	chr2:234547400-234547800	Enhancers	NHEK	skin
32	chr2:234547400-234548200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr2:234547400-234548200	Enhancers	HMEC	breast
34	chr2:234547600-234548200	Enhancers	Duodenum Mucosa	Duodenum
35	chr2:234547800-234554000	Weak transcription	Colonic Mucosa	Colon
36	chr2:234548000-234548200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr2:234548200-234548800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr2:234548200-234549400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr2:234548400-234549000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr2:234549400-234550000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr2:234549400-234550000	Enhancers	Stomach Mucosa	stomach
42	chr2:234550000-234551400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr2:234550000-234551400	Weak transcription	Stomach Mucosa	stomach
44	chr2:234551400-234551600	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr2:234551400-234551800	Enhancers	Stomach Mucosa	stomach
46	chr2:234551600-234551800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:234551600-234551800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:234551600-234551800	Enhancers	Esophagus	oesophagus
49	chr2:234551600-234553800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr2:234551800-234559200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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