Variant report

Variant	esv2756933
Chromosome Location	chr2:78199735-78640246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:906)
CpG islands
(count:123)
Chromatin interactive
region (count:26)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:906 , 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	chr2:78336522-78336700	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:78532952-78532953	K562	blood:	n/a	n/a
3	ARID3A	chr2:78578413-78578720	K562	blood:	n/a	n/a
4	ARID3A	chr2:78361077-78361118	K562	blood:	n/a	n/a
5	ARID3A	chr2:78389314-78389802	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:78487915-78488675	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:78413821-78414186	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:78578391-78578636	HepG2	liver:	n/a	n/a
9	ATF1	chr2:78361002-78361126	K562	blood:	n/a	n/a
10	ATF1	chr2:78215207-78215394	K562	blood:	n/a	n/a
11	ATF1	chr2:78408127-78408325	K562	blood:	n/a	n/a
12	BACH1	chr2:78477710-78477711	K562	blood:	n/a	n/a
13	BACH1	chr2:78368178-78368199	K562	blood:	n/a	n/a
14	BATF	chr2:78428253-78428380	GM12878	blood:	n/a	n/a
15	BATF	chr2:78508306-78508624	GM12878	blood:	n/a	n/a
16	BATF	chr2:78508305-78508535	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:78508311-78508495	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:78263040-78263247	H1-hESC	embryonic stem cell:	n/a	n/a
19	BHLHE40	chr2:78487986-78488343	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:78490807-78490864	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:78508455-78508636	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:78389461-78389669	HepG2	liver:	n/a	n/a
23	CBX3	chr2:78256529-78256863	K562	blood:	n/a	n/a
24	CBX3	chr2:78256534-78256829	K562	blood:	n/a	n/a
25	CBX3	chr2:78273160-78273446	K562	blood:	n/a	n/a
26	CBX3	chr2:78273156-78273427	K562	blood:	n/a	n/a
27	CCNT2	chr2:78252676-78252871	K562	blood:	n/a	n/a
28	CEBPB	chr2:78207174-78207351	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:78257848-78257981	HepG2	liver:	n/a	chr2:78257886-78257897
30	CEBPB	chr2:78420675-78420797	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:78537183-78537401	K562	blood:	n/a	n/a
32	CEBPB	chr2:78413736-78414060	A549	lung:	n/a	chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413881-78413894 chr2:78413882-78413893 chr2:78413881-78413894 chr2:78413881-78413892 chr2:78413883-78413892
33	CEBPB	chr2:78589467-78589821	K562	blood:	n/a	chr2:78589637-78589648
34	CEBPB	chr2:78204592-78204931	K562	blood:	n/a	n/a
35	CEBPB	chr2:78518559-78518875	IMR90	lung:	n/a	chr2:78518707-78518718
36	CEBPB	chr2:78359219-78359536	MCF-7	breast:	n/a	n/a
37	CEBPB	chr2:78583349-78583384	K562	blood:	n/a	n/a
38	CEBPB	chr2:78589546-78589687	H1-hESC	embryonic stem cell:	n/a	chr2:78589637-78589648
39	CEBPB	chr2:78200278-78200392	H1-hESC	embryonic stem cell:	n/a	chr2:78200332-78200343
40	CEBPB	chr2:78445215-78445558	K562	blood:	n/a	chr2:78445380-78445391
41	CEBPB	chr2:78589542-78589761	IMR90	lung:	n/a	chr2:78589637-78589648
42	CEBPB	chr2:78200255-78200411	IMR90	lung:	n/a	chr2:78200332-78200343
43	CEBPB	chr2:78445211-78445551	A549	lung:	n/a	chr2:78445380-78445391
44	CEBPB	chr2:78278630-78278975	A549	lung:	n/a	chr2:78278787-78278798
45	CEBPB	chr2:78560369-78560622	A549	lung:	n/a	chr2:78560467-78560478
46	CEBPB	chr2:78275962-78276210	IMR90	lung:	n/a	chr2:78276047-78276058
47	CEBPB	chr2:78420619-78420902	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:78445210-78445573	HepG2	liver:	n/a	chr2:78445380-78445391
49	CEBPB	chr2:78413713-78414071	HepG2	liver:	n/a	chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413881-78413894 chr2:78413882-78413893 chr2:78413881-78413894 chr2:78413881-78413892 chr2:78413883-78413892
50	CEBPB	chr2:78369163-78369459	HepG2	liver:	n/a	chr2:78369346-78369359 chr2:78369367-78369378

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78263008-78263058	AG09319	gingival:	n/a
2	chr2:78263008-78263058	AG09319	gingival:	n/a
3	chr2:78263008-78263058	BE2_C	brain:	n/a
4	chr2:78263008-78263058	HRE	kidney:	n/a
5	chr2:78263008-78263058	H1-hESC	embryonic stem cell:	embryo
6	chr2:78263008-78263058	GM12891	blood:	n/a
7	chr2:78545567-78545617	ProgFib	skin:	n/a
8	chr2:78263008-78263058	SK-N-SH_RA	brain:	n/a
9	chr2:78545567-78545617	HEEpiC	esophagus:	n/a
10	chr2:78263008-78263058	Hepatocyte	liver:	n/a
11	chr2:78263008-78263058	Hela-S3	cervix:	n/a
12	chr2:78545567-78545617	HCT-116	colon:	n/a
13	chr2:78545567-78545617	A549	lung:	n/a
14	chr2:78545567-78545617	ovcar-3	ovarian:	n/a
15	chr2:78263008-78263058	BJ	skin:	n/a
16	chr2:78263008-78263058	AG09309	skin:	n/a
17	chr2:78263008-78263058	ovcar-3	ovarian:	n/a
18	chr2:78545567-78545617	MCF10A-Er-Src	breast:	n/a
19	chr2:78545567-78545617	AoSMC	blood vessel:	n/a
20	chr2:78263008-78263058	CMK	blood:	n/a
21	chr2:78545567-78545617	ECC-1	luminal epithelium:	n/a
22	chr2:78263008-78263058	AG04450	lung:	fetal
23	chr2:78545567-78545617	HRCEpiC	kidney:	n/a
24	chr2:78545567-78545617	T-47D	breast:	n/a
25	chr2:78545567-78545617	HRE	kidney:	n/a
26	chr2:78545567-78545617	MCF-7	breast:	n/a
27	chr2:78263008-78263058	HAEpiC	amniotic membrane:	n/a
28	chr2:78263008-78263058	NHBE	bronchial:	n/a
29	chr2:78263008-78263058	NB4	blood:	n/a
30	chr2:78545567-78545617	SAEC	small airway:	n/a
31	chr2:78545567-78545617	HepG2	liver:	n/a
32	chr2:78545567-78545617	PrEC	prostate:	n/a
33	chr2:78545567-78545617	SK-N-SH	brain:	n/a
34	chr2:78545567-78545617	HMEC	breast:	n/a
35	chr2:78545567-78545617	HNPCEpiC	eye:	n/a
36	chr2:78545567-78545617	LNCaP	prostate:	n/a
37	chr2:78263008-78263058	SK-N-SH	brain:	n/a
38	chr2:78545567-78545617	Hela-S3	cervix:	n/a
39	chr2:78545567-78545617	IMR90	lung:	fetal
40	chr2:78545567-78545617	Jurkat	blood:	n/a
41	chr2:78545567-78545617	GM12878	blood:	n/a
42	chr2:78545567-78545617	AG09319	gingival:	n/a
43	chr2:78263008-78263058	HRCEpiC	kidney:	n/a
44	chr2:78545567-78545617	BJ	skin:	n/a
45	chr2:78263008-78263058	T-47D	breast:	n/a
46	chr2:78545567-78545617	PFSK-1	brain:	n/a
47	chr2:78263008-78263058	HCF	heart:	n/a
48	chr2:78263008-78263058	HCT-116	colon:	n/a
49	chr2:78545567-78545617	HIPEpiC	eye:	n/a
50	chr2:78263008-78263058	AG04449	skin:	fetal

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:78637554..78639977-chr2:78766787..78768860,2	K562	blood:
2	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
3	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
4	chr2:78607954..78609567-chr2:78764622..78766807,2	K562	blood:
5	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
6	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
7	chr17:59624355..59624932-chr2:78345304..78345966,2	MCF-7	breast:
8	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
9	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
10	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
11	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
12	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
13	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
14	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
15	chr2:78578454..78579130-chr2:79226516..79227199,2	MCF-7	breast:
16	chr2:78577011..78577791-chr8:96157456..96158424,2	MCF-7	breast:
17	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
18	chr2:78578299..78578916-chr2:79206809..79207351,2	MCF-7	breast:
19	chr2:78215424..78217099-chr2:78219299..78221415,2	K562	blood:
20	chr2:78577613..78578539-chr2:79206466..79207847,3	MCF-7	breast:
21	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
22	chr2:78519747..78522682-chr2:78785137..78786876,2	K562	blood:
23	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
24	chr2:78215424..78217099-chr2:78219299..78221415,2	K562	blood:
25	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
26	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRTM4-3	chr2:78225204-78225307	NONHSAT071835
2	lnc-REG3G-3	chr2:78322790-78322968	XLOC_001543
3	lnc-LRRTM4-3	chr2:78229100-78229271	NONHSAT071835
4	lnc-REG3G-8	chr2:78208133-78208440	NONHSAT071839
5	lnc-LRRTM4-3	chr2:78639673-78640302	NONHSAT071846
6	lnc-LRRTM4-8	chr2:78371022-78371323	ucscGeneNc_uc002snu_2
7	lnc-LRRTM4-3	chr2:78637204-78640302	NONHSAT071835
8	lnc-LRRTM4-3	chr2:78639919-78640220	NONHSAT071847
9	lnc-LRRTM4-3	chr2:78214578-78215904	NONHSAT071835
10	lnc-REG3G-3	chr2:78320703-78320792	XLOC_001543
11	lnc-REG3G-3	chr2:78339185-78339226	XLOC_001543
12	lnc-LRRTM4-3	chr2:78517514-78517857	NR_110288
13	lnc-REG3G-3	chr2:78321763-78321902	XLOC_001543
14	lnc-REG3G-3	chr2:78354625-78354877	XLOC_001543
15	lnc-LRRTM4-3	chr2:78252450-78252550	NONHSAT071835

No data

Variant related genes	Relation type
CYCSP6	TF binding region
ENSG00000229494	TF binding region
CYCSP6	CpG island
ENSG00000229494	CpG island

Extended variants
information (count: 7572 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7572 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1527184	chr2:78199735-78199736	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570719296	chr2:78199736-78199737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112864662	chr2:78199738-78199739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543757263	chr2:78199739-78199740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142937253	chr2:78199805-78199806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532854227	chr2:78199814-78199815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540452887	chr2:78199824-78199825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76625255	chr2:78199842-78199843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529232795	chr2:78199858-78199859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549287295	chr2:78199878-78199879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569135156	chr2:78199910-78199911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531742201	chr2:78199948-78199949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116556150	chr2:78199978-78199979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556657688	chr2:78200002-78200003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568826975	chr2:78200009-78200010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180902854	chr2:78200018-78200019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74697607	chr2:78200043-78200044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs207461905	chr2:78200062-78200063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542774386	chr2:78200085-78200086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554372747	chr2:78200115-78200116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536332808	chr2:78200120-78200121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561264863	chr2:78200121-78200122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185462273	chr2:78200140-78200141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369964607	chr2:78200148-78200149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76141911	chr2:78200160-78200161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74404849	chr2:78200161-78200162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572796063	chr2:78200179-78200180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190961426	chr2:78200218-78200219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs62166562	chr2:78200220-78200221	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs144697024	chr2:78200238-78200239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371836922	chr2:78200240-78200241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181364574	chr2:78200256-78200257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138555339	chr2:78200274-78200275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563663584	chr2:78200308-78200309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116328165	chr2:78200333-78200334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs62166563	chr2:78200413-78200414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs199694433	chr2:78200445-78200446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1527183	chr2:78200451-78200452	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573892675	chr2:78200516-78200517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533007997	chr2:78200522-78200523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542798685	chr2:78200541-78200542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114862381	chr2:78200580-78200581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547834300	chr2:78200590-78200591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567531408	chr2:78200594-78200595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531605427	chr2:78200614-78200615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6712046	chr2:78200615-78200616	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549899624	chr2:78200619-78200620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530164395	chr2:78200651-78200652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186392006	chr2:78200671-78200672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62166564	chr2:78200703-78200704	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78195200-78200200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr2:78199200-78201800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:78199600-78200200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr2:78199800-78200000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr2:78200000-78200400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:78200000-78200800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr2:78200200-78200400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:78200200-78201200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:78200400-78200600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr2:78200400-78201400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr2:78200600-78201000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:78200600-78201800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:78200800-78201200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:78200800-78201600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:78201200-78201400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:78201200-78201400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:78201400-78201800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:78201400-78202000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:78201400-78204200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:78204600-78205000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:78220200-78220800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:78226200-78226800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr2:78226200-78227000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:78226600-78227400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:78226800-78227200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr2:78227200-78227400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr2:78227400-78229200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr2:78229200-78229400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr2:78229400-78229800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr2:78229800-78230200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr2:78237000-78237200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:78237200-78238200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr2:78238000-78238400	Active TSS	Brain Substantia Nigra	brain
34	chr2:78238200-78238400	Enhancers	Brain Cingulate Gyrus	brain
35	chr2:78238200-78238600	Active TSS	Brain Angular Gyrus	brain
36	chr2:78238200-78240800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:78238400-78238800	Active TSS	Brain Cingulate Gyrus	brain
38	chr2:78239400-78239600	Enhancers	Brain Cingulate Gyrus	brain
39	chr2:78243000-78253200	Weak transcription	HepG2	liver
40	chr2:78250400-78251000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr2:78251800-78254000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr2:78254000-78254200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
43	chr2:78255800-78257600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:78259000-78259800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr2:78259800-78262400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:78260600-78261600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr2:78261600-78261800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr2:78261800-78262400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr2:78261800-78263600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr2:78261800-78263800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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