Variant report

Variant	esv3397779
Chromosome Location	chr5:180019946-180024344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:68)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:68 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr5:180022112-180022394	GM12878	blood:	n/a	n/a
2	BCL3	chr5:180021796-180022349	GM12878	blood:	n/a	n/a
3	CBX3	chr5:180021566-180021935	K562	blood:	n/a	n/a
4	CEBPB	chr5:180023747-180024336	MCF-7	breast:	n/a	n/a
5	CTCF	chr5:180022400-180022550	SAEC	small airway:	n/a	n/a
6	CTCF	chr5:180022681-180022691	LNCaP	prostate:	n/a	n/a
7	CTCF	chr5:180023960-180024110	HepG2	liver:	n/a	n/a
8	CTCF	chr5:180023932-180023998	MCF-7	breast:	n/a	n/a
9	CTCF	chr5:180023966-180023977	LNCaP	prostate:	n/a	n/a
10	CTCF	chr5:180022693-180022722	LNCaP	prostate:	n/a	n/a
11	CTCF	chr5:180023942-180024009	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:180022665-180022732	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:180023938-180023998	MCF-7	breast:	n/a	n/a
14	EGR1	chr5:180021690-180022123	GM12878	blood:	n/a	n/a
15	EGR1	chr5:180021494-180022404	K562	blood:	n/a	n/a
16	EGR1	chr5:180021750-180022049	GM12878	blood:	n/a	n/a
17	EGR1	chr5:180021526-180022460	K562	blood:	n/a	n/a
18	EGR1	chr5:180021582-180022502	MCF-7	breast:	n/a	n/a
19	ELF1	chr5:180023782-180024390	MCF-7	breast:	n/a	n/a
20	EP300	chr5:180022472-180023049	T-47D	breast:	n/a	chr5:180022779-180022789
21	EP300	chr5:180023550-180024261	T-47D	breast:	n/a	chr5:180023658-180023674 chr5:180024007-180024016
22	EP300	chr5:180023702-180024210	T-47D	breast:	n/a	chr5:180024007-180024016
23	EP300	chr5:180022504-180022989	T-47D	breast:	n/a	chr5:180022779-180022789
24	EP300	chr5:180022470-180022918	MCF-7	breast:	n/a	chr5:180022779-180022789
25	ESR1	chr5:180022399-180023116	T-47D	breast:	n/a	chr5:180022733-180022750
26	ESR1	chr5:180023633-180024325	T-47D	breast:	n/a	n/a
27	ESR1	chr5:180022416-180023357	T-47D	breast:	n/a	chr5:180022733-180022750
28	ESR1	chr5:180023686-180024306	T-47D	breast:	n/a	n/a
29	ESR1	chr5:180023554-180024404	T-47D	breast:	n/a	n/a
30	ESR1	chr5:180022454-180023104	T-47D	breast:	n/a	chr5:180022733-180022750
31	ESR1	chr5:180023597-180024341	T-47D	breast:	n/a	n/a
32	ESR1	chr5:180022491-180023005	T-47D	breast:	n/a	chr5:180022733-180022750
33	ESR1	chr5:180022340-180023144	T-47D	breast:	n/a	chr5:180022733-180022750
34	ESR1	chr5:180023578-180024416	T-47D	breast:	n/a	n/a
35	ESR1	chr5:180023610-180024357	T-47D	breast:	n/a	n/a
36	ESR1	chr5:180022344-180023152	T-47D	breast:	n/a	chr5:180022733-180022750
37	FOXA1	chr5:180023782-180024090	HepG2	liver:	n/a	n/a
38	FOXA1	chr5:180022529-180023004	T-47D	breast:	n/a	chr5:180022778-180022793 chr5:180022829-180022844
39	FOXA1	chr5:180023026-180023292	T-47D	breast:	n/a	n/a
40	FOXA1	chr5:180022635-180023037	T-47D	breast:	n/a	chr5:180022778-180022793 chr5:180022829-180022844
41	FOXA1	chr5:180023730-180024189	T-47D	breast:	n/a	n/a
42	FOXA1	chr5:180023702-180024224	T-47D	breast:	n/a	n/a
43	FOXA1	chr5:180023792-180024165	HepG2	liver:	n/a	n/a
44	FOXA2	chr5:180023819-180024074	HepG2	liver:	n/a	n/a
45	FOXA2	chr5:180023730-180024247	A549	lung:	n/a	n/a
46	GATA3	chr5:180022583-180022973	T-47D	breast:	n/a	n/a
47	GATA3	chr5:180022474-180023018	MCF-7	breast:	n/a	n/a
48	GATA3	chr5:180023746-180024204	T-47D	breast:	n/a	n/a
49	GATA3	chr5:180023724-180024117	T-47D	breast:	n/a	n/a
50	GATA3	chr5:180022541-180023027	T-47D	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180021235-180021285	K562	blood:	n/a
2	chr5:180021235-180021285	K562	blood:	n/a
3	chr5:180021235-180021285	NHDF-neo	bronchial:	n/a
4	chr5:180022909-180022959	GM12891	blood:	n/a
5	chr5:180022909-180022959	HCT-116	colon:	n/a
6	chr5:180022909-180022959	PFSK-1	brain:	n/a
7	chr5:180022909-180022959	GM12878	blood:	n/a
8	chr5:180021235-180021285	HNPCEpiC	eye:	n/a
9	chr5:180021235-180021285	AG09309	skin:	n/a
10	chr5:180022909-180022959	PrEC	prostate:	n/a
11	chr5:180021235-180021285	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:180022909-180022959	SK-N-MC	brain:	n/a
13	chr5:180021235-180021285	Jurkat	blood:	n/a
14	chr5:180021235-180021285	HRPEpiC	eye:	n/a
15	chr5:180022909-180022959	GM12892	blood:	n/a
16	chr5:180021235-180021285	SAEC	small airway:	n/a
17	chr5:180022909-180022959	Hela-S3	cervix:	n/a
18	chr5:180022909-180022959	NB4	blood:	n/a
19	chr5:180022909-180022959	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:180021235-180021285	BJ	skin:	n/a
21	chr5:180022909-180022959	HCM	heart:	n/a
22	chr5:180021235-180021285	GM12878	blood:	n/a
23	chr5:180022909-180022959	NHDF-neo	bronchial:	n/a
24	chr5:180021235-180021285	ProgFib	skin:	n/a
25	chr5:180021235-180021285	AG10803	skin:	n/a
26	chr5:180022909-180022959	Hepatocyte	liver:	n/a
27	chr5:180021235-180021285	HMEC	breast:	n/a
28	chr5:180021235-180021285	NT2-D1	testis:	n/a
29	chr5:180021235-180021285	HIPEpiC	eye:	n/a
30	chr5:180021235-180021285	HL-60	blood:	n/a
31	chr5:180021235-180021285	GM12892	blood:	n/a
32	chr5:180021235-180021285	H1-hESC	embryonic stem cell:	embryo
33	chr5:180021235-180021285	ECC-1	luminal epithelium:	n/a
34	chr5:180022909-180022959	NHBE	bronchial:	n/a
35	chr5:180021235-180021285	AG04449	skin:	fetal
36	chr5:180022909-180022959	HCF	heart:	n/a
37	chr5:180022909-180022959	MCF10A-Er-Src	breast:	n/a
38	chr5:180022909-180022959	MCF-7	breast:	n/a
39	chr5:180022909-180022959	HRCEpiC	kidney:	n/a
40	chr5:180022909-180022959	T-47D	breast:	n/a
41	chr5:180022909-180022959	NH-A	brain:	n/a
42	chr5:180022909-180022959	HRE	kidney:	n/a
43	chr5:180021235-180021285	SK-N-SH_RA	brain:	n/a
44	chr5:180021235-180021285	AoSMC	blood vessel:	n/a
45	chr5:180022909-180022959	SK-N-SH	brain:	n/a
46	chr5:180022909-180022959	A549	lung:	n/a
47	chr5:180021235-180021285	HEK293	kidney:	embryo
48	chr5:180021235-180021285	Caco-2	colon:	n/a
49	chr5:180021235-180021285	HRCEpiC	kidney:	n/a
50	chr5:180021235-180021285	IMR90	lung:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:180016834..180019339-chr5:180022480..180024182,5	MCF-7	breast:
2	chr5:177543208..177543993-chr5:180022726..180023297,2	MCF-7	breast:
3	chr5:180024110..180026371-chr5:180028713..180030538,2	K562	blood:
4	chr5:180016309..180018997-chr5:180020974..180022491,2	K562	blood:
5	chr5:179719112..179720727-chr5:180023144..180025071,2	MCF-7	breast:
6	chr5:179925282..179927939-chr5:180022784..180024577,2	K562	blood:
7	chr5:180015126..180018318-chr5:180024001..180027146,3	K562	blood:
8	chr5:180012397..180015247-chr5:180019489..180021552,2	MCF-7	breast:
9	chr5:180022631..180025317-chr5:180096101..180098291,2	MCF-7	breast:
10	chr5:179739596..179742574-chr5:180022400..180024079,2	MCF-7	breast:

No data

Variant related genes	Relation type
SCGB3A1	TF binding region
SCGB3A1	CpG island
ENSG00000161055	chromatin interactions
ENSG00000248367	chromatin interactions

Extended variants
information (count: 186 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:186 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565538599	chr5:180019951-180019952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs307804	chr5:180019952-180019953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548747701	chr5:180019964-180019965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568532024	chr5:180019999-180020000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534162768	chr5:180020033-180020034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547951399	chr5:180020034-180020035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542475803	chr5:180020102-180020103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571083200	chr5:180020144-180020145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564824360	chr5:180020224-180020225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185074993	chr5:180020225-180020226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558142036	chr5:180020286-180020287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568466837	chr5:180020309-180020310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115710514	chr5:180020372-180020373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554282283	chr5:180020390-180020391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574458419	chr5:180020427-180020428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147047682	chr5:180020474-180020475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148081913	chr5:180020492-180020493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190623090	chr5:180020495-180020496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546074387	chr5:180020516-180020517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs80111099	chr5:180020575-180020576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541640416	chr5:180020592-180020593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531780710	chr5:180020612-180020613	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192954203	chr5:180020618-180020619	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534656291	chr5:180020619-180020620	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527761167	chr5:180020633-180020634	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547690902	chr5:180020667-180020668	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570987171	chr5:180020668-180020669	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142027726	chr5:180020671-180020672	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150275729	chr5:180020733-180020734	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570002489	chr5:180020771-180020772	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537480765	chr5:180020851-180020852	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554527786	chr5:180020925-180020926	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs72816982	chr5:180020952-180020953	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12652622	chr5:180020960-180020961	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185210901	chr5:180020997-180020998	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553693419	chr5:180020998-180020999	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563434526	chr5:180021006-180021007	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189845444	chr5:180021015-180021016	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546013464	chr5:180021038-180021039	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs138930701	chr5:180021071-180021072	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576383554	chr5:180021097-180021098	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs10053714	chr5:180021099-180021100	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs55672724	chr5:180021151-180021152	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs146350975	chr5:180021273-180021274	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541470488	chr5:180021281-180021282	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374125033	chr5:180021290-180021291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564419276	chr5:180021294-180021295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139887028	chr5:180021316-180021317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141632661	chr5:180021368-180021369	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74603820	chr5:180021406-180021407	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180018400-180021400	Weak transcription	Pancreas	Pancrea
2	chr5:180018800-180045800	Weak transcription	Right Atrium	heart
3	chr5:180019000-180021600	Weak transcription	Gastric	stomach
4	chr5:180019000-180022600	Weak transcription	Spleen	Spleen
5	chr5:180019600-180020800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:180020600-180020800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr5:180020600-180020800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr5:180020800-180021200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:180021200-180021400	Enhancers	K562	blood
10	chr5:180021200-180021800	Enhancers	Fetal Thymus	thymus
11	chr5:180021200-180022400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:180021400-180021800	Flanking Active TSS	K562	blood
13	chr5:180021400-180022400	Enhancers	Pancreas	Pancrea
14	chr5:180021600-180021800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
15	chr5:180021600-180024000	Enhancers	Gastric	stomach
16	chr5:180021800-180022000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:180021800-180022000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
18	chr5:180021800-180022400	Enhancers	K562	blood
19	chr5:180021800-180023000	Enhancers	Lung	lung
20	chr5:180022000-180023200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:180022400-180022600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:180022400-180022800	Flanking Active TSS	Pancreas	Pancrea
23	chr5:180022400-180023000	Enhancers	Liver	Liver
24	chr5:180022600-180022800	ZNF genes & repeats	Spleen	Spleen
25	chr5:180022600-180023800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:180022800-180024200	Enhancers	Pancreas	Pancrea
27	chr5:180022800-180024800	Weak transcription	Spleen	Spleen
28	chr5:180023600-180023800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:180023800-180024000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr5:180023800-180024000	Enhancers	Fetal Thymus	thymus
31	chr5:180023800-180024200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:180023800-180024200	Enhancers	Placenta	Placenta
33	chr5:180024000-180024200	Bivalent Enhancer	HepG2	liver
34	chr5:180024000-180039000	Weak transcription	Gastric	stomach
35	chr5:180024200-180025000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:180024200-180032800	Weak transcription	Placenta	Placenta

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