Variant report

Variant	esv3368938
Chromosome Location	chr8:103449847-103469656
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	ATF2	chr8:103468031-103468409	GM12878	blood:	n/a	n/a
2	ATF2	chr8:103467906-103468376	GM12878	blood:	n/a	n/a
3	BHLHE40	chr8:103468029-103468368	GM12878	blood:	n/a	n/a
4	BHLHE40	chr8:103466435-103466518	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:103456507-103456791	K562	blood:	n/a	chr8:103456653-103456664
6	CEBPB	chr8:103459138-103459332	A549	lung:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
7	CEBPB	chr8:103456501-103456812	HepG2	liver:	n/a	chr8:103456653-103456664
8	CEBPB	chr8:103463105-103463118	A549	lung:	n/a	n/a
9	CEBPB	chr8:103459051-103459333	K562	blood:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
10	CEBPB	chr8:103459025-103459378	HepG2	liver:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
11	CEBPB	chr8:103459129-103459282	HepG2	liver:	n/a	chr8:103459195-103459204 chr8:103459195-103459206 chr8:103459193-103459204
12	CEBPB	chr8:103456528-103456757	K562	blood:	n/a	chr8:103456653-103456664
13	CHD1	chr8:103466390-103466405	GM12878	blood:	n/a	n/a
14	CTCF	chr8:103454390-103454420	Lung_OC	lung:	n/a	n/a
15	CTCF	chr8:103464318-103464407	Lung_OC	lung:	n/a	n/a
16	CTCF	chr8:103462548-103462598	GM20000	blood:	n/a	n/a
17	CTCF	chr8:103456953-103456978	GM10266	blood:	n/a	n/a
18	CTCF	chr8:103456982-103456985	GM10266	blood:	n/a	n/a
19	EP300	chr8:103468163-103468228	GM12878	blood:	n/a	n/a
20	EP300	chr8:103466415-103466543	GM12878	blood:	n/a	chr8:103466514-103466528
21	EP300	chr8:103468111-103468326	GM12878	blood:	n/a	n/a
22	FAM48A	chr8:103450611-103450615	GM12878	blood:	n/a	n/a
23	FOXA1	chr8:103469279-103469465	T-47D	breast:	n/a	n/a
24	FOXA2	chr8:103456366-103456497	HepG2	liver:	n/a	n/a
25	FOXM1	chr8:103467982-103468449	GM12878	blood:	n/a	n/a
26	FOXM1	chr8:103468049-103468605	GM12878	blood:	n/a	n/a
27	GATA1	chr8:103456171-103456886	K562	blood:	n/a	n/a
28	GATA2	chr8:103453246-103453601	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr8:103453218-103453703	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr8:103453188-103453724	SK-N-SH	brain:	n/a	n/a
31	IKZF1	chr8:103469122-103469422	GM12878	blood:	n/a	n/a
32	JUND	chr8:103462225-103462374	K562	blood:	n/a	chr8:103462313-103462324
33	JUND	chr8:103456333-103456619	K562	blood:	n/a	n/a
34	JUND	chr8:103462198-103462398	HepG2	liver:	n/a	chr8:103462313-103462324
35	MAX	chr8:103456368-103456444	K562	blood:	n/a	n/a
36	MEF2A	chr8:103467880-103468411	GM12878	blood:	n/a	n/a
37	MYC	chr8:103461053-103461194	H1-hESC	embryonic stem cell:	n/a	n/a
38	MYC	chr8:103466979-103466986	MCF10A-Er-Src	breast:	n/a	n/a
39	NFATC1	chr8:103468045-103468413	GM12878	blood:	n/a	n/a
40	NFIC	chr8:103467996-103468468	GM12878	blood:	n/a	n/a
41	NFIC	chr8:103466255-103466734	GM12878	blood:	n/a	n/a
42	NFIC	chr8:103467924-103468423	GM12878	blood:	n/a	n/a
43	POLR2A	chr8:103457721-103457790	ProgFib	skin:	n/a	n/a
44	POLR2A	chr8:103464371-103464496	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr8:103467004-103467265	K562	blood:	n/a	n/a
46	POLR2A	chr8:103458366-103458460	K562	blood:	n/a	n/a
47	POLR2A	chr8:103460127-103460264	K562	blood:	n/a	n/a
48	POLR2A	chr8:103455117-103455212	K562	blood:	n/a	n/a
49	POLR2A	chr8:103464613-103464690	K562	blood:	n/a	n/a
50	POLR2A	chr8:103466002-103466134	ProgFib	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:103448154..103449973-chr8:103656128..103658488,2	MCF-7	breast:
2	chr8:103422125..103426655-chr8:103454292..103458691,6	MCF-7	breast:
3	chr8:103432099..103434551-chr8:103448773..103451141,2	MCF-7	breast:
4	chr17:57919324..57922033-chr8:103458324..103460694,2	MCF-7	breast:
5	chr8:103439421..103441100-chr8:103448054..103450571,2	MCF-7	breast:
6	chr8:103436437..103439478-chr8:103450415..103454144,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KB-1980E6.3.1-3	chr8:103463991-103464240	NONHSAT128096
2	lnc-KB-1980E6.3.1-3	chr8:103464660-103464711	NONHSAT128096

Variant related genes	Relation type
HSPE1P14	TF binding region
ENSG00000104517	chromatin interactions
ENSG00000221387	chromatin interactions

Extended variants
information (count: 504 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113720965	chr8:103449862-103449863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs182166106	chr8:103449873-103449874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567249494	chr8:103449908-103449909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571810324	chr8:103449985-103449986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs116696394	chr8:103450001-103450002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572402696	chr8:103450026-103450027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148467013	chr8:103450054-103450055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs117405308	chr8:103450074-103450075	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574361448	chr8:103450085-103450086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529923138	chr8:103450087-103450088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs543398367	chr8:103450112-103450113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371561533	chr8:103450133-103450134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs144895288	chr8:103450182-103450183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375078039	chr8:103450183-103450184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185169085	chr8:103450193-103450194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs57231146	chr8:103450216-103450217	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557501518	chr8:103450240-103450241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548483458	chr8:103450241-103450242	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534168421	chr8:103450270-103450271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs563287761	chr8:103450275-103450276	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554868794	chr8:103450295-103450296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs7836803	chr8:103450304-103450305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7836807	chr8:103450309-103450310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139794156	chr8:103450338-103450339	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577242510	chr8:103450363-103450364	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559539107	chr8:103450423-103450424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs143188862	chr8:103450438-103450439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs530736558	chr8:103450442-103450443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs4621773	chr8:103450455-103450456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs116968842	chr8:103450550-103450551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs62523144	chr8:103450602-103450603	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs368982109	chr8:103450630-103450631	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368314789	chr8:103450681-103450682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528405606	chr8:103450706-103450707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546572667	chr8:103450726-103450727	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs117069303	chr8:103450741-103450742	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530850344	chr8:103450773-103450774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146676320	chr8:103450792-103450793	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116554250	chr8:103450828-103450829	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569410159	chr8:103450980-103450981	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs536491176	chr8:103450981-103450982	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs554830097	chr8:103450990-103450991	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566094839	chr8:103451049-103451050	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs9694458	chr8:103451073-103451074	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558491395	chr8:103451092-103451093	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188763794	chr8:103451120-103451121	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34816253	chr8:103451137-103451138	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs9693239	chr8:103451141-103451142	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181907413	chr8:103451159-103451160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372958034	chr8:103451211-103451212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Autism	22495309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103447200-103450800	Enhancers	H1 Cell Line	embryonic stem cell
2	chr8:103448400-103453400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:103448800-103450400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:103449600-103450000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:103449600-103450600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr8:103449600-103450800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:103449600-103451000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr8:103449600-103453000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:103449600-103453000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:103449800-103450800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:103449800-103450800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr8:103449800-103453200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:103450000-103450400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr8:103450400-103451200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:103450600-103450800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr8:103450600-103451200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:103450800-103451000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr8:103450800-103451200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:103450800-103451200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:103450800-103451200	Enhancers	A549	lung
21	chr8:103450800-103452600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:103451000-103453200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr8:103453000-103453200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr8:103453000-103453600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:103453000-103453600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:103453200-103453400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:103453200-103453600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr8:103453400-103453600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr8:103455800-103456200	Enhancers	K562	blood
30	chr8:103456000-103456600	Enhancers	Placenta	Placenta
31	chr8:103456200-103456600	Flanking Active TSS	K562	blood
32	chr8:103456600-103456800	Enhancers	K562	blood
33	chr8:103459200-103459400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:103459400-103459600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr8:103465600-103467800	Enhancers	GM12878-XiMat	blood
36	chr8:103467800-103468400	Flanking Active TSS	GM12878-XiMat	blood
37	chr8:103468400-103468800	Enhancers	GM12878-XiMat	blood
38	chr8:103468600-103469600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr8:103468600-103471800	Weak transcription	Hela-S3	cervix
40	chr8:103468800-103469000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr8:103468800-103469400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr8:103468800-103469400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr8:103468800-103469400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:103468800-103469400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr8:103468800-103469400	Enhancers	Stomach Smooth Muscle	stomach
46	chr8:103468800-103469600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr8:103468800-103469600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr8:103468800-103470000	Flanking Active TSS	GM12878-XiMat	blood
49	chr8:103469000-103469400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr8:103469000-103469400	Enhancers	K562	blood

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