Variant report

Variant	esv2752990
Chromosome Location	chr2:77038541-77217310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:77122571-77123208	HepG2	liver:	n/a	n/a
2	BACH1	chr2:77097162-77097483	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr2:77167917-77167935	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:77180986-77181204	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:77202307-77202452	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:77180978-77181201	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr2:77180931-77181241	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr2:77063314-77063462	HepG2	liver:	n/a	chr2:77063403-77063414
9	CEBPB	chr2:77052964-77053028	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:77122603-77122971	A549	lung:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
11	CEBPB	chr2:77122547-77122985	MCF-7	breast:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
12	CEBPB	chr2:77122556-77122880	HepG2	liver:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
13	CEBPB	chr2:77172470-77172928	A549	lung:	n/a	chr2:77172758-77172771 chr2:77172626-77172637 chr2:77172758-77172769 chr2:77172758-77172769 chr2:77172625-77172638
14	CEBPB	chr2:77105143-77105334	HepG2	liver:	n/a	chr2:77105158-77105169
15	CEBPB	chr2:77122593-77122972	Hela-S3	cervix:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
16	CEBPB	chr2:77172472-77172742	HepG2	liver:	n/a	chr2:77172626-77172637 chr2:77172625-77172638
17	CEBPB	chr2:77122537-77123013	A549	lung:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
18	CEBPB	chr2:77122604-77122992	HepG2	liver:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
19	CEBPB	chr2:77122611-77122887	ECC-1	luminal epithelium:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
20	CEBPB	chr2:77061836-77062064	HepG2	liver:	n/a	chr2:77061951-77061964 chr2:77061951-77061962 chr2:77061885-77061897 chr2:77061952-77061963
21	CEBPB	chr2:77122595-77122980	MCF-7	breast:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
22	CEBPB	chr2:77063392-77063498	A549	lung:	n/a	chr2:77063403-77063414
23	CEBPB	chr2:77130594-77130778	HepG2	liver:	n/a	chr2:77130612-77130623
24	CEBPB	chr2:77122644-77122941	A549	lung:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
25	CEBPB	chr2:77122605-77122963	H1-hESC	embryonic stem cell:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
26	CEBPB	chr2:77180727-77181209	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:77122614-77122855	K562	blood:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
28	CEBPB	chr2:77048855-77049199	HepG2	liver:	n/a	chr2:77049026-77049037
29	CEBPB	chr2:77203949-77204214	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:77055418-77055648	HepG2	liver:	n/a	chr2:77055485-77055496
31	CEBPB	chr2:77122593-77122967	IMR90	lung:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
32	CEBPB	chr2:77122524-77122982	HepG2	liver:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
33	CEBPB	chr2:77079155-77079453	HepG2	liver:	n/a	chr2:77079276-77079287 chr2:77079278-77079287 chr2:77079278-77079287 chr2:77079278-77079289 chr2:77079276-77079289 chr2:77079278-77079287 chr2:77079278-77079287
34	CEBPB	chr2:77097382-77098085	IMR90	lung:	n/a	chr2:77097736-77097749 chr2:77097733-77097750
35	CEBPB	chr2:77122629-77122889	HepG2	liver:	n/a	chr2:77122779-77122788 chr2:77122777-77122790 chr2:77122779-77122788 chr2:77122779-77122788 chr2:77122777-77122788 chr2:77122779-77122788
36	CEBPD	chr2:77122634-77122892	HepG2	liver:	n/a	chr2:77122779-77122788
37	CHD1	chr2:77071814-77071830	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr2:77088801-77089173	GM12878	blood:	n/a	n/a
39	CREB1	chr2:77088795-77089187	GM12878	blood:	n/a	n/a
40	CTCF	chr2:77180915-77181164	A549	lung:	n/a	n/a
41	CTCF	chr2:77180942-77181174	GM10266	blood:	n/a	n/a
42	CTCF	chr2:77170500-77170650	HepG2	liver:	n/a	n/a
43	CTCF	chr2:77180954-77181139	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr2:77180980-77181130	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr2:77167505-77167550	GM10266	blood:	n/a	n/a
46	CTCF	chr2:77180980-77181130	NHEK	skin:	n/a	n/a
47	CTCF	chr2:77180911-77181175	LNCaP	prostate:	n/a	n/a
48	CTCF	chr2:77180980-77181130	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr2:77180860-77181010	AG09309	skin:	n/a	n/a
50	CTCF	chr2:77097260-77097410	HPF	lung:	n/a	chr2:77097344-77097357 chr2:77097342-77097360

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77038948-77038998	GM06990	blood:	n/a
2	chr2:77038948-77038998	ECC-1	luminal epithelium:	n/a
3	chr2:77038948-77038998	PrEC	prostate:	n/a
4	chr2:77038948-77038998	HUVEC	blood vessel:	n/a
5	chr2:77038948-77038998	U87	brain:	n/a
6	chr2:77038948-77038998	AG10803	skin:	n/a
7	chr2:77038948-77038998	Hela-S3	cervix:	n/a
8	chr2:77038948-77038998	LNCaP	prostate:	n/a
9	chr2:77038948-77038998	K562	blood:	n/a
10	chr2:77038948-77038998	H1-hESC	embryonic stem cell:	embryo
11	chr2:77038948-77038998	SAEC	small airway:	n/a
12	chr2:77038948-77038998	GM12892	blood:	n/a
13	chr2:77038948-77038998	CMK	blood:	n/a
14	chr2:77038948-77038998	RPTEC	kidney:	n/a
15	chr2:77038948-77038998	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:77038948-77038998	MCF10A-Er-Src	breast:	n/a
17	chr2:77038948-77038998	NB4	blood:	n/a
18	chr2:77038948-77038998	HIPEpiC	eye:	n/a
19	chr2:77038948-77038998	AG09309	skin:	n/a
20	chr2:77038948-77038998	A549	lung:	n/a
21	chr2:77038948-77038998	AG09319	gingival:	n/a
22	chr2:77038948-77038998	AG04449	skin:	fetal
23	chr2:77038948-77038998	BJ	skin:	n/a
24	chr2:77038948-77038998	HMEC	breast:	n/a
25	chr2:77038948-77038998	SK-N-SH	brain:	n/a
26	chr2:77038948-77038998	HEK293	kidney:	embryo
27	chr2:77038948-77038998	NHDF-neo	bronchial:	n/a
28	chr2:77038948-77038998	Hepatocyte	liver:	n/a
29	chr2:77038948-77038998	T-47D	breast:	n/a
30	chr2:77038948-77038998	HNPCEpiC	eye:	n/a
31	chr2:77038948-77038998	NH-A	brain:	n/a
32	chr2:77038948-77038998	SK-N-MC	brain:	n/a
33	chr2:77038948-77038998	HepG2	liver:	n/a
34	chr2:77038948-77038998	SKMC	muscle:	n/a
35	chr2:77038948-77038998	HCM	heart:	n/a
36	chr2:77038948-77038998	Caco-2	colon:	n/a
37	chr2:77038948-77038998	IMR90	lung:	fetal
38	chr2:77038948-77038998	NT2-D1	testis:	n/a
39	chr2:77038948-77038998	ovcar-3	ovarian:	n/a
40	chr2:77038948-77038998	GM12891	blood:	n/a
41	chr2:77038948-77038998	PFSK-1	brain:	n/a
42	chr2:77038948-77038998	PANC-1	pancreas:	n/a
43	chr2:77038948-77038998	HRE	kidney:	n/a
44	chr2:77038948-77038998	HCPEpiC	choroid plexus:	n/a
45	chr2:77038948-77038998	AoSMC	blood vessel:	n/a
46	chr2:77038948-77038998	SK-N-SH_RA	brain:	n/a
47	chr2:77038948-77038998	HCT-116	colon:	n/a
48	chr2:77038948-77038998	NHBE	bronchial:	n/a
49	chr2:77038948-77038998	MCF-7	breast:	n/a
50	chr2:77038948-77038998	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:77048830..77049446-chr2:77059405..77060125,2	MCF-7	breast:
2	chr2:77040309..77042734-chr2:77044070..77045998,2	K562	blood:
3	chr2:77116319..77118650-chr2:77122168..77124589,2	K562	blood:
4	chr2:77179669..77181456-chr2:77188236..77191117,3	K562	blood:
5	chr2:77116319..77118650-chr2:77122168..77124589,2	K562	blood:
6	chr2:77179669..77181456-chr2:77188236..77191117,3	K562	blood:
7	chr2:77048830..77049446-chr2:77059405..77060125,2	MCF-7	breast:
8	chr2:77111498..77113879-chr21:46359661..46361542,2	MCF-7	breast:
9	chr2:77040309..77042734-chr2:77044070..77045998,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL19-4	chr2:77213091-77213127	ENSG00000234653.1
2	lnc-MRPL19-4	chr2:77214532-77214620	ENSG00000234653.1
3	lnc-MRPL19-4	chr2:77216947-77217052	NR_110284
4	lnc-MRPL19-4	chr2:77214532-77214620	NR_110284
5	lnc-MRPL19-4	chr2:77213091-77213127	NR_110284
6	lnc-MRPL19-4	chr2:77216947-77217052	ENSG00000234653.1

Variant related genes	Relation type
ENSG00000234653	TF binding region
ENSG00000234653	CpG island
ENSG00000160256	chromatin interactions
ENSG00000183250	chromatin interactions

Extended variants
information (count: 4594 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4594 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1400846	chr2:77038541-77038542	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550416245	chr2:77038556-77038557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562460702	chr2:77038589-77038590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532832142	chr2:77038625-77038626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114675688	chr2:77038632-77038633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570842058	chr2:77038673-77038674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534866024	chr2:77038716-77038717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546761605	chr2:77038721-77038722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141722347	chr2:77038741-77038742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535902413	chr2:77038756-77038757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557177974	chr2:77038797-77038798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537163846	chr2:77038799-77038800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539876919	chr2:77038805-77038806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555315305	chr2:77038831-77038832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146961480	chr2:77038839-77038840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80209204	chr2:77038846-77038847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138046949	chr2:77038854-77038855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540550262	chr2:77038855-77038856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113321301	chr2:77038895-77038896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540419387	chr2:77038896-77038897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573760292	chr2:77038897-77038898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544294400	chr2:77038921-77038922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562482076	chr2:77038949-77038950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4516455	chr2:77038986-77038987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550988234	chr2:77038998-77038999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531114565	chr2:77039015-77039016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559737403	chr2:77039016-77039017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528727500	chr2:77039017-77039018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546898968	chr2:77039018-77039019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568592971	chr2:77039020-77039021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149053298	chr2:77039029-77039030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143051660	chr2:77039068-77039069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569279592	chr2:77039069-77039070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573677711	chr2:77039109-77039110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558147951	chr2:77039117-77039118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541066969	chr2:77039127-77039128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566879354	chr2:77039141-77039142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561994347	chr2:77039158-77039159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148190746	chr2:77039162-77039163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77326604	chr2:77039168-77039169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573774034	chr2:77039208-77039209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544115680	chr2:77039270-77039271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141355251	chr2:77039276-77039277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191859899	chr2:77039311-77039312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544720874	chr2:77039322-77039323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184104782	chr2:77039339-77039340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370691038	chr2:77039340-77039341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146257784	chr2:77039345-77039346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578189496	chr2:77039348-77039349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138045873	chr2:77039349-77039350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Epilepsy	22083797	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77009000-77039000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:77036200-77041800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr2:77036600-77038600	Weak transcription	Fetal Kidney	kidney
4	chr2:77038200-77039000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:77038200-77039600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:77038200-77040200	Enhancers	Fetal Lung	lung
7	chr2:77038400-77038600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:77038400-77039800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:77038600-77039200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr2:77038600-77039400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:77038600-77039400	Enhancers	Fetal Kidney	kidney
12	chr2:77039000-77039400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:77039200-77039400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr2:77039200-77039400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:77039200-77039600	Enhancers	Colon Smooth Muscle	Colon
16	chr2:77039400-77039600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:77039400-77042200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr2:77039600-77039800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:77039600-77042200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr2:77039600-77049600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:77039800-77041800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr2:77040000-77041800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:77041800-77042600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr2:77041800-77042800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr2:77041800-77043400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:77042200-77042800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:77042200-77042800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:77048600-77048800	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr2:77049400-77049600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr2:77050800-77051200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:77051200-77051400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr2:77051200-77052400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr2:77051400-77051600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr2:77052400-77053000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:77052600-77052800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:77052600-77052800	Weak transcription	Psoas Muscle	Psoas
37	chr2:77052800-77053000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr2:77052800-77053000	ZNF genes & repeats	Psoas Muscle	Psoas
39	chr2:77052800-77053200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:77053000-77054000	Weak transcription	Psoas Muscle	Psoas
41	chr2:77053800-77054600	Enhancers	Brain Cingulate Gyrus	brain
42	chr2:77054000-77054200	Enhancers	Psoas Muscle	Psoas
43	chr2:77054000-77054600	Enhancers	Brain Hippocampus Middle	brain
44	chr2:77055400-77056000	Enhancers	Brain Anterior Caudate	brain
45	chr2:77055600-77056000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr2:77055600-77056200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr2:77066400-77067800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:77067000-77067600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:77067000-77067800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:77067000-77067800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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