Variant report

Variant	esv34157
Chromosome Location	chr2:73901718-73949151
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:926)
CpG islands
(count:489)
Chromatin interactive
region (count:22)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73944205-73944414	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
3	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
4	ATF1	chr2:73928292-73928546	K562	blood:	n/a	n/a
5	ATF1	chr2:73943828-73944353	K562	blood:	n/a	n/a
6	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
7	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
8	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
10	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
11	BATF	chr2:73917830-73918048	GM12878	blood:	n/a	n/a
12	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
14	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:73928154-73928613	K562	blood:	n/a	n/a
16	BHLHE40	chr2:73933790-73934083	K562	blood:	n/a	n/a
17	BHLHE40	chr2:73917955-73917976	K562	blood:	n/a	n/a
18	CBX3	chr2:73925209-73925579	K562	blood:	n/a	n/a
19	CBX3	chr2:73925299-73925547	K562	blood:	n/a	n/a
20	CBX3	chr2:73944839-73945197	K562	blood:	n/a	n/a
21	CBX3	chr2:73943935-73944537	K562	blood:	n/a	n/a
22	CBX3	chr2:73928047-73928946	K562	blood:	n/a	n/a
23	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
24	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
25	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73927189-73927886	MCF-7	breast:	n/a	chr2:73927522-73927535
27	CEBPB	chr2:73927361-73927552	HepG2	liver:	n/a	chr2:73927522-73927535
28	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
29	CEBPB	chr2:73940735-73940928	K562	blood:	n/a	chr2:73940777-73940788
30	CEBPB	chr2:73926566-73926627	A549	lung:	n/a	n/a
31	CEBPB	chr2:73940714-73941127	IMR90	lung:	n/a	chr2:73940777-73940788
32	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73927206-73927852	MCF-7	breast:	n/a	chr2:73927522-73927535
34	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
35	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
36	CEBPB	chr2:73940681-73941130	A549	lung:	n/a	chr2:73940777-73940788
37	CEBPB	chr2:73940640-73941075	HepG2	liver:	n/a	chr2:73940777-73940788
38	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
39	CTCF	chr2:73918020-73918170	GM12873	blood:	n/a	n/a
40	CTCF	chr2:73907363-73907637	K562	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
41	CTCF	chr2:73912160-73912310	GM12878	blood:	n/a	n/a
42	CTCF	chr2:73917920-73918070	GM12867	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
43	CTCF	chr2:73907321-73907685	K562	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
44	CTCF	chr2:73912240-73912390	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr2:73917540-73917690	HVMF	connective:	n/a	n/a
46	CTCF	chr2:73907300-73907708	H1-hESC	embryonic stem cell:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
47	CTCF	chr2:73912260-73912410	HMF	breast:	n/a	n/a
48	CTCF	chr2:73907360-73907510	HMEC	breast:	n/a	n/a
49	CTCF	chr2:73921088-73921176	GM20000	blood:	n/a	n/a
50	CTCF	chr2:73917910-73918068	SK-N-SH_RA	brain:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73907327-73907377	PFSK-1	brain:	n/a
2	chr2:73907327-73907377	PFSK-1	brain:	n/a
3	chr2:73928492-73928542	AoSMC	blood vessel:	n/a
4	chr2:73907327-73907377	HMEC	breast:	n/a
5	chr2:73929892-73929942	HCM	heart:	n/a
6	chr2:73929765-73929815	HEK293	kidney:	embryo
7	chr2:73928500-73928550	Hepatocyte	liver:	n/a
8	chr2:73907327-73907377	NT2-D1	testis:	n/a
9	chr2:73928500-73928550	HepG2	liver:	n/a
10	chr2:73927710-73927760	AG09309	skin:	n/a
11	chr2:73927710-73927760	MCF-7	breast:	n/a
12	chr2:73927710-73927760	HCT-116	colon:	n/a
13	chr2:73928492-73928542	LNCaP	prostate:	n/a
14	chr2:73907327-73907377	SKMC	muscle:	n/a
15	chr2:73928492-73928542	HL-60	blood:	n/a
16	chr2:73928348-73928398	SK-N-SH	brain:	n/a
17	chr2:73929765-73929815	ECC-1	luminal epithelium:	n/a
18	chr2:73907327-73907377	ProgFib	skin:	n/a
19	chr2:73929634-73929684	HRPEpiC	eye:	n/a
20	chr2:73929892-73929942	HRPEpiC	eye:	n/a
21	chr2:73928492-73928542	HCPEpiC	choroid plexus:	n/a
22	chr2:73928348-73928398	NHBE	bronchial:	n/a
23	chr2:73928348-73928398	H1-hESC	embryonic stem cell:	embryo
24	chr2:73929634-73929684	BE2_C	brain:	n/a
25	chr2:73929765-73929815	SK-N-SH_RA	brain:	n/a
26	chr2:73928492-73928542	PANC-1	pancreas:	n/a
27	chr2:73929765-73929815	Jurkat	blood:	n/a
28	chr2:73928348-73928398	T-47D	breast:	n/a
29	chr2:73927710-73927760	CMK	blood:	n/a
30	chr2:73929765-73929815	NH-A	brain:	n/a
31	chr2:73928492-73928542	GM12892	blood:	n/a
32	chr2:73927710-73927760	HRPEpiC	eye:	n/a
33	chr2:73928492-73928542	U87	brain:	n/a
34	chr2:73929765-73929815	Hepatocyte	liver:	n/a
35	chr2:73928348-73928398	HepG2	liver:	n/a
36	chr2:73907327-73907377	K562	blood:	n/a
37	chr2:73929765-73929815	A549	lung:	n/a
38	chr2:73929892-73929942	AG09309	skin:	n/a
39	chr2:73907327-73907377	HIPEpiC	eye:	n/a
40	chr2:73929892-73929942	HRCEpiC	kidney:	n/a
41	chr2:73928348-73928398	SKMC	muscle:	n/a
42	chr2:73929892-73929942	ECC-1	luminal epithelium:	n/a
43	chr2:73929892-73929942	IMR90	lung:	fetal
44	chr2:73927710-73927760	IMR90	lung:	fetal
45	chr2:73927710-73927760	PFSK-1	brain:	n/a
46	chr2:73929634-73929684	BJ	skin:	n/a
47	chr2:73929765-73929815	AG04449	skin:	fetal
48	chr2:73929634-73929684	CMK	blood:	n/a
49	chr2:73907327-73907377	Caco-2	colon:	n/a
50	chr2:73928492-73928542	HMEC	breast:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
2	chr2:73928399..73931050-chr2:73932225..73934947,2	K562	blood:
3	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
4	chr2:73943613..73945709-chr2:73953816..73955383,2	MCF-7	breast:
5	chr2:73932554..73934998-chr2:74005796..74007372,2	MCF-7	breast:
6	chr2:73940417..73941921-chr2:73955171..73957279,2	MCF-7	breast:
7	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
8	chr2:73931503..73934295-chr2:73936024..73937687,2	MCF-7	breast:
9	chr2:73927692..73931050-chr2:73931884..73934947,3	K562	blood:
10	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
11	chr2:73931503..73934295-chr2:73936024..73937687,2	MCF-7	breast:
12	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
13	chr2:73934784..73936668-chr2:73963156..73965791,2	K562	blood:
14	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
15	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
16	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
17	chr2:73934847..73936533-chr2:73939356..73942331,2	K562	blood:
18	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
19	chr2:73934847..73936533-chr2:73939356..73942331,2	K562	blood:
20	chr2:73945415..73947505-chr2:73953398..73955264,2	K562	blood:
21	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
22	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf78-1	chr2:73933639-73934687	ENSG00000251346
2	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
3	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
4	lnc-C2orf78-1	chr2:73927556-73928129	ENSG00000251346

No data

Variant related genes	Relation type
ENSG00000204872	TF binding region
ENSG00000204872	CpG island
ENSG00000144035	chromatin interactions
ENSG00000204872	chromatin interactions
ENSG00000163016	chromatin interactions
ENSG00000144048	chromatin interactions
ENSG00000144034	chromatin interactions
UBE2I	miRNA target sites

Extended variants
information (count: 2195 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2195 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548041882	chr2:73901785-73901786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35671590	chr2:73901787-73901788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35389986	chr2:73901794-73901795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563247621	chr2:73901894-73901895	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555805785	chr2:73901904-73901905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530608818	chr2:73901926-73901927	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551986138	chr2:73901937-73901938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570188026	chr2:73901942-73901943	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373255662	chr2:73901977-73901978	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs200040304	chr2:73901980-73901981	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs189885628	chr2:73902029-73902030	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs201019923	chr2:73902031-73902032	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs201713318	chr2:73902032-73902033	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs373275644	chr2:73902040-73902041	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568007400	chr2:73902230-73902231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35457528	chr2:73902261-73902262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535107262	chr2:73902297-73902298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557685302	chr2:73902304-73902305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576050013	chr2:73902311-73902312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376305857	chr2:73902313-73902314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558418619	chr2:73902322-73902323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573381730	chr2:73902323-73902324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567726206	chr2:73902372-73902373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555590868	chr2:73902383-73902384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376810001	chr2:73902414-73902415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182202269	chr2:73902418-73902419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370699446	chr2:73902440-73902441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550195891	chr2:73902446-73902447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139629735	chr2:73902458-73902459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4511748	chr2:73902491-73902492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564271381	chr2:73902544-73902545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186384342	chr2:73902548-73902549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144175922	chr2:73902559-73902560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568108012	chr2:73902571-73902572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528873574	chr2:73902580-73902581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370280627	chr2:73902638-73902639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550632004	chr2:73902664-73902665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569550655	chr2:73902677-73902678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146058567	chr2:73902684-73902685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558504753	chr2:73902723-73902724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115933698	chr2:73902725-73902726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534135198	chr2:73902728-73902729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555829146	chr2:73902739-73902740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574082328	chr2:73902754-73902755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544176381	chr2:73902808-73902809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115526607	chr2:73902975-73902976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577628739	chr2:73902981-73902982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34211121	chr2:73902996-73902997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545651746	chr2:73902999-73903000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564226642	chr2:73903015-73903016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73896200-73905200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:73897200-73904600	Weak transcription	Gastric	stomach
3	chr2:73898600-73903600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr2:73899200-73902200	Weak transcription	Fetal Brain Male	brain
5	chr2:73899400-73902000	Weak transcription	Aorta	Aorta
6	chr2:73899400-73902800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:73899600-73902000	Weak transcription	Fetal Lung	lung
8	chr2:73899800-73902200	Strong transcription	Brain Anterior Caudate	brain
9	chr2:73900600-73912800	Weak transcription	Liver	Liver
10	chr2:73900600-73913000	Weak transcription	Pancreas	Pancrea
11	chr2:73900600-73954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr2:73901200-73903400	Weak transcription	Fetal Brain Female	brain
13	chr2:73901400-73905200	Weak transcription	Brain Angular Gyrus	brain
14	chr2:73901400-73913000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:73901600-73911400	Weak transcription	Ovary	ovary
16	chr2:73901800-73902400	Enhancers	GM12878-XiMat	blood
17	chr2:73902200-73931400	Weak transcription	Brain Anterior Caudate	brain
18	chr2:73905200-73905600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:73906200-73907000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr2:73906800-73909600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:73907000-73907400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr2:73907000-73907400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr2:73907200-73907400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr2:73907200-73907400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:73907200-73907400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:73911400-73911600	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr2:73911400-73911800	Enhancers	Ovary	ovary
28	chr2:73911800-73912800	Weak transcription	Ovary	ovary
29	chr2:73911800-73913000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr2:73912600-73913000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr2:73912800-73913200	Enhancers	HepG2	liver
32	chr2:73912800-73913600	Enhancers	Ovary	ovary
33	chr2:73912800-73913600	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr2:73912800-73914200	Enhancers	Liver	Liver
35	chr2:73912800-73914200	Enhancers	Fetal Intestine Large	intestine
36	chr2:73912800-73914200	Enhancers	Fetal Intestine Small	intestine
37	chr2:73912800-73914600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:73913000-73913200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:73913000-73913400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
40	chr2:73913000-73913400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
41	chr2:73913000-73913400	Active TSS	Duodenum Mucosa	Duodenum
42	chr2:73913000-73913600	Enhancers	Gastric	stomach
43	chr2:73913000-73913600	Enhancers	Pancreas	Pancrea
44	chr2:73913000-73913600	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr2:73913000-73913600	Enhancers	Stomach Mucosa	stomach
46	chr2:73913000-73914200	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr2:73913000-73914200	Enhancers	Primary hematopoietic stem cells	blood
48	chr2:73913000-73914200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr2:73913000-73914200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr2:73913200-73913600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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