Variant report

Variant	esv34750
Chromosome Location	chr2:78251145-78434845
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:373)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:78389314-78389802	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:78336522-78336700	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:78413821-78414186	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:78361077-78361118	K562	blood:	n/a	n/a
5	ATF1	chr2:78408127-78408325	K562	blood:	n/a	n/a
6	ATF1	chr2:78361002-78361126	K562	blood:	n/a	n/a
7	BACH1	chr2:78368178-78368199	K562	blood:	n/a	n/a
8	BATF	chr2:78428253-78428380	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:78263040-78263247	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr2:78389461-78389669	HepG2	liver:	n/a	n/a
11	CBX3	chr2:78273160-78273446	K562	blood:	n/a	n/a
12	CBX3	chr2:78256529-78256863	K562	blood:	n/a	n/a
13	CBX3	chr2:78256534-78256829	K562	blood:	n/a	n/a
14	CBX3	chr2:78273156-78273427	K562	blood:	n/a	n/a
15	CCNT2	chr2:78252676-78252871	K562	blood:	n/a	n/a
16	CEBPB	chr2:78278630-78278975	A549	lung:	n/a	chr2:78278787-78278798
17	CEBPB	chr2:78336457-78336666	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:78278661-78278923	H1-hESC	embryonic stem cell:	n/a	chr2:78278787-78278798
19	CEBPB	chr2:78335197-78335393	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:78278654-78278947	K562	blood:	n/a	chr2:78278787-78278798
21	CEBPB	chr2:78275962-78276210	IMR90	lung:	n/a	chr2:78276047-78276058
22	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
23	CEBPB	chr2:78336524-78336852	A549	lung:	n/a	n/a
24	CEBPB	chr2:78275936-78276189	HepG2	liver:	n/a	chr2:78276047-78276058
25	CEBPB	chr2:78336445-78336815	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:78336390-78336918	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:78278610-78278979	HepG2	liver:	n/a	chr2:78278787-78278798
28	CEBPB	chr2:78376053-78376336	HepG2	liver:	n/a	chr2:78376191-78376202
29	CEBPB	chr2:78257848-78257981	HepG2	liver:	n/a	chr2:78257886-78257897
30	CEBPB	chr2:78369163-78369459	HepG2	liver:	n/a	chr2:78369346-78369359 chr2:78369367-78369378
31	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
32	CEBPB	chr2:78336457-78336742	K562	blood:	n/a	n/a
33	CEBPB	chr2:78359219-78359536	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:78420675-78420797	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:78420652-78420781	K562	blood:	n/a	n/a
36	CEBPB	chr2:78336473-78336839	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:78389473-78389661	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:78336515-78336886	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:78288591-78288834	HepG2	liver:	n/a	chr2:78288709-78288720
40	CEBPB	chr2:78389426-78389688	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:78400416-78400616	HepG2	liver:	n/a	chr2:78400485-78400496
42	CEBPB	chr2:78420619-78420902	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:78278617-78278979	IMR90	lung:	n/a	chr2:78278787-78278798
44	CEBPB	chr2:78336403-78336930	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:78359289-78359640	MCF-7	breast:	n/a	n/a
46	CEBPD	chr2:78336473-78336816	HepG2	liver:	n/a	n/a
47	CEBPZ	chr2:78333011-78333129	HepG2	liver:	n/a	n/a
48	CHD2	chr2:78272055-78272174	K562	blood:	n/a	n/a
49	CHD2	chr2:78271928-78272084	GM12878	blood:	n/a	n/a
50	CHD2	chr2:78333169-78333316	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78263008-78263058	HCT-116	colon:	n/a
2	chr2:78263008-78263058	HCM	heart:	n/a
3	chr2:78263008-78263058	GM12878	blood:	n/a
4	chr2:78263008-78263058	ProgFib	skin:	n/a
5	chr2:78263008-78263058	NB4	blood:	n/a
6	chr2:78263008-78263058	HMEC	breast:	n/a
7	chr2:78263008-78263058	HEEpiC	esophagus:	n/a
8	chr2:78263008-78263058	SK-N-SH_RA	brain:	n/a
9	chr2:78263008-78263058	NHDF-neo	bronchial:	n/a
10	chr2:78263008-78263058	LNCaP	prostate:	n/a
11	chr2:78263008-78263058	IMR90	lung:	fetal
12	chr2:78263008-78263058	SK-N-MC	brain:	n/a
13	chr2:78263008-78263058	HepG2	liver:	n/a
14	chr2:78263008-78263058	AG10803	skin:	n/a
15	chr2:78263008-78263058	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:78263008-78263058	HRCEpiC	kidney:	n/a
17	chr2:78263008-78263058	Hepatocyte	liver:	n/a
18	chr2:78263008-78263058	Caco-2	colon:	n/a
19	chr2:78263008-78263058	PFSK-1	brain:	n/a
20	chr2:78263008-78263058	HCPEpiC	choroid plexus:	n/a
21	chr2:78263008-78263058	H1-hESC	embryonic stem cell:	embryo
22	chr2:78263008-78263058	GM12892	blood:	n/a
23	chr2:78263008-78263058	HCF	heart:	n/a
24	chr2:78263008-78263058	BE2_C	brain:	n/a
25	chr2:78263008-78263058	K562	blood:	n/a
26	chr2:78263008-78263058	ovcar-3	ovarian:	n/a
27	chr2:78263008-78263058	AG04450	lung:	fetal
28	chr2:78263008-78263058	Jurkat	blood:	n/a
29	chr2:78263008-78263058	PANC-1	pancreas:	n/a
30	chr2:78263008-78263058	NHBE	bronchial:	n/a
31	chr2:78263008-78263058	GM19239	blood:	n/a
32	chr2:78263008-78263058	GM12891	blood:	n/a
33	chr2:78263008-78263058	SK-N-SH	brain:	n/a
34	chr2:78263008-78263058	AoSMC	blood vessel:	n/a
35	chr2:78263008-78263058	HRE	kidney:	n/a
36	chr2:78263008-78263058	HNPCEpiC	eye:	n/a
37	chr2:78263008-78263058	HRPEpiC	eye:	n/a
38	chr2:78263008-78263058	MCF10A-Er-Src	breast:	n/a
39	chr2:78263008-78263058	A549	lung:	n/a
40	chr2:78263008-78263058	HL-60	blood:	n/a
41	chr2:78263008-78263058	Hela-S3	cervix:	n/a
42	chr2:78263008-78263058	SKMC	muscle:	n/a
43	chr2:78263008-78263058	GM06990	blood:	n/a
44	chr2:78263008-78263058	HEK293	kidney:	embryo
45	chr2:78263008-78263058	HUVEC	blood vessel:	n/a
46	chr2:78263008-78263058	NH-A	brain:	n/a
47	chr2:78263008-78263058	MCF-7	breast:	n/a
48	chr2:78263008-78263058	PrEC	prostate:	n/a
49	chr2:78263008-78263058	RPTEC	kidney:	n/a
50	chr2:78263008-78263058	U87	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
2	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
3	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
4	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
5	chr17:59624355..59624932-chr2:78345304..78345966,2	MCF-7	breast:
6	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
7	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
8	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
9	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
10	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
11	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-3	chr2:78320703-78320792	XLOC_001543
2	lnc-LRRTM4-8	chr2:78371022-78371323	ucscGeneNc_uc002snu_2
3	lnc-REG3G-3	chr2:78321763-78321902	XLOC_001543
4	lnc-REG3G-3	chr2:78339185-78339226	XLOC_001543
5	lnc-LRRTM4-3	chr2:78252450-78252550	NONHSAT071835
6	lnc-REG3G-3	chr2:78354625-78354877	XLOC_001543
7	lnc-REG3G-3	chr2:78322790-78322968	XLOC_001543

No data

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

Extended variants
information (count: 3575 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3575 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9973347	chr2:78251191-78251192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184494210	chr2:78251234-78251235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542547079	chr2:78251239-78251240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190185760	chr2:78251281-78251282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182192175	chr2:78251308-78251309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149940113	chr2:78251318-78251319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9973351	chr2:78251337-78251338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs548431604	chr2:78251338-78251339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527796195	chr2:78251353-78251354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575287236	chr2:78251360-78251361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187269697	chr2:78251445-78251446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530303665	chr2:78251446-78251447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145008899	chr2:78251477-78251478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570250793	chr2:78251489-78251490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149078413	chr2:78251502-78251503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111478225	chr2:78251529-78251530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143712120	chr2:78251628-78251629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180702933	chr2:78251629-78251630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185277708	chr2:78251631-78251632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560315819	chr2:78251635-78251636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200172582	chr2:78251672-78251673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369375568	chr2:78251697-78251698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553433746	chr2:78251720-78251721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146565474	chr2:78251742-78251743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536032725	chr2:78251790-78251791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555751875	chr2:78251795-78251796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72817242	chr2:78251798-78251799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576266874	chr2:78251840-78251841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs13397799	chr2:78251862-78251863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13397888	chr2:78251865-78251866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114942349	chr2:78251879-78251880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367889510	chr2:78251882-78251883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558704744	chr2:78251908-78251909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112209670	chr2:78251930-78251931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541573580	chr2:78251982-78251983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561358623	chr2:78251983-78251984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113927208	chr2:78251997-78251998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10203046	chr2:78252024-78252025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs563867507	chr2:78252073-78252074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144985778	chr2:78252087-78252088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552812413	chr2:78252104-78252105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564760291	chr2:78252111-78252112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116522673	chr2:78252164-78252165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375365063	chr2:78252176-78252177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190434982	chr2:78252261-78252262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571353320	chr2:78252266-78252267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139032260	chr2:78252268-78252269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78199526	chr2:78252275-78252276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10205479	chr2:78252297-78252298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs62164371	chr2:78252323-78252324	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

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
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

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78243000-78253200	Weak transcription	HepG2	liver
2	chr2:78251800-78254000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr2:78254000-78254200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
4	chr2:78255800-78257600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:78259000-78259800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr2:78259800-78262400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:78260600-78261600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:78261600-78261800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:78261800-78262400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr2:78261800-78263600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr2:78261800-78263800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:78261800-78263800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:78261800-78263800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:78262000-78263000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr2:78262400-78262800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr2:78262400-78263200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:78262600-78263600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:78262800-78263000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr2:78262800-78263400	Enhancers	H9 Cell Line	embryonic stem cell
20	chr2:78263000-78263400	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr2:78263200-78263600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr2:78263400-78263800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr2:78263600-78263800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr2:78263800-78264000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr2:78263800-78264800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:78265000-78265200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:78270800-78271000	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr2:78271000-78272200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr2:78272800-78274200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:78282400-78284000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:78286000-78289600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr2:78288200-78288600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:78288200-78288800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr2:78288200-78288800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr2:78288200-78289000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:78288200-78289400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:78288400-78289200	Enhancers	Fetal Muscle Leg	muscle
38	chr2:78288400-78289600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr2:78288600-78289600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:78288800-78289200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr2:78289600-78293200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:78293200-78293400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:78295800-78296200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr2:78296200-78305400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr2:78298000-78298800	Enhancers	Fetal Lung	lung
46	chr2:78301200-78306400	Weak transcription	HepG2	liver
47	chr2:78303600-78305600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:78304600-78305600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:78305000-78305200	Enhancers	Brain Substantia Nigra	brain
50	chr2:78305000-78305400	Enhancers	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links