Variant report

Variant	esv16734
Chromosome Location	chr15:74347110-74402574
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	chr15:74392408-74392650	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr15:74392349-74392641	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr15:74392413-74392721	GM12878	blood:	n/a	chr15:74392614-74392623
4	ATF3	chr15:74392398-74392716	H1-hESC	embryonic stem cell:	n/a	chr15:74392614-74392623
5	ATF3	chr15:74392450-74392694	K562	blood:	n/a	chr15:74392614-74392623
6	ATF3	chr15:74392430-74392628	HepG2	liver:	n/a	chr15:74392614-74392623
7	ATF3	chr15:74392455-74392650	GM12878	blood:	n/a	chr15:74392614-74392623
8	ATF3	chr15:74392349-74392672	HepG2	liver:	n/a	chr15:74392614-74392623
9	ATF3	chr15:74392359-74392646	H1-hESC	embryonic stem cell:	n/a	chr15:74392614-74392623
10	BACH1	chr15:74392468-74392664	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr15:74401844-74402047	GM12878	blood:	n/a	n/a
12	BATF	chr15:74358070-74358340	GM12878	blood:	n/a	n/a
13	BATF	chr15:74378602-74378908	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:74374739-74374923	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:74371726-74371899	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:74392492-74392788	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:74358034-74358288	GM12878	blood:	n/a	n/a
18	BCL3	chr15:74392422-74392635	GM12878	blood:	n/a	n/a
19	BCL3	chr15:74392429-74392639	GM12878	blood:	n/a	n/a
20	BCLAF1	chr15:74392425-74392718	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:74392395-74392664	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:74392465-74392715	GM12878	blood:	n/a	chr15:74392614-74392623 chr15:74392612-74392625 chr15:74392615-74392624 chr15:74392608-74392629 chr15:74392614-74392623
23	BHLHE40	chr15:74392412-74392803	HepG2	liver:	n/a	chr15:74392614-74392623 chr15:74392612-74392625 chr15:74392615-74392624 chr15:74392608-74392629 chr15:74392614-74392623
24	BHLHE40	chr15:74392513-74392741	HepG2	liver:	n/a	chr15:74392614-74392623 chr15:74392612-74392625 chr15:74392615-74392624 chr15:74392608-74392629 chr15:74392614-74392623
25	BHLHE40	chr15:74392501-74392718	K562	blood:	n/a	chr15:74392614-74392623 chr15:74392612-74392625 chr15:74392615-74392624 chr15:74392608-74392629 chr15:74392614-74392623
26	BRCA1	chr15:74392505-74392707	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr15:74392515-74392663	GM12878	blood:	n/a	n/a
28	CBX3	chr15:74392270-74392719	K562	blood:	n/a	n/a
29	CBX3	chr15:74358099-74358712	K562	blood:	n/a	n/a
30	CBX3	chr15:74392136-74392829	K562	blood:	n/a	n/a
31	CEBPB	chr15:74402091-74402405	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:74392389-74393039	GM12878	blood:	n/a	chr15:74392793-74392810
33	CHD2	chr15:74392365-74392741	HepG2	liver:	n/a	n/a
34	CHD2	chr15:74392510-74392709	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr15:74392380-74392723	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr15:74392351-74392735	GM12878	blood:	n/a	n/a
37	CHD2	chr15:74392378-74392729	K562	blood:	n/a	n/a
38	CREB1	chr15:74392403-74392652	A549	lung:	n/a	n/a
39	CTCF	chr15:74358200-74358350	HCT-116	colon:	n/a	chr15:74358265-74358283 chr15:74358267-74358288 chr15:74358268-74358281 chr15:74358266-74358282 chr15:74358268-74358277
40	CTCF	chr15:74400960-74401110	GM12870	blood:	n/a	n/a
41	CTCF	chr15:74365420-74365570	GM06990	blood:	n/a	n/a
42	CTCF	chr15:74358220-74358370	BJ	skin:	n/a	chr15:74358265-74358283 chr15:74358267-74358288 chr15:74358268-74358281 chr15:74358266-74358282 chr15:74358268-74358277
43	CTCF	chr15:74401020-74401170	GM12870	blood:	n/a	n/a
44	CTCF	chr15:74357960-74358110	GM12864	blood:	n/a	n/a
45	CTCF	chr15:74401051-74401239	K562	blood:	n/a	n/a
46	CTCF	chr15:74385624-74385673	LNCaP	prostate:	n/a	n/a
47	CTCF	chr15:74401080-74401230	GM12867	blood:	n/a	n/a
48	CTCF	chr15:74401048-74401301	K562	blood:	n/a	n/a
49	CTCF	chr15:74392433-74392520	GM10248	blood:	n/a	n/a
50	CTCF	chr15:74365376-74365537	GM12891	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74392505-74392555	ProgFib	skin:	n/a
2	chr15:74365539-74365589	AG04449	skin:	fetal
3	chr15:74365101-74365151	PrEC	prostate:	n/a
4	chr15:74392505-74392555	HCT-116	colon:	n/a
5	chr15:74396537-74396587	Hela-S3	cervix:	n/a
6	chr15:74365501-74365551	HCF	heart:	n/a
7	chr15:74365101-74365151	GM12878	blood:	n/a
8	chr15:74396537-74396587	HEEpiC	esophagus:	n/a
9	chr15:74365501-74365551	U87	brain:	n/a
10	chr15:74392505-74392555	Jurkat	blood:	n/a
11	chr15:74365539-74365589	H1-hESC	embryonic stem cell:	embryo
12	chr15:74392612-74392662	HAEpiC	amniotic membrane:	n/a
13	chr15:74392612-74392662	NHBE	bronchial:	n/a
14	chr15:74392612-74392662	HepG2	liver:	n/a
15	chr15:74357886-74357936	HepG2	liver:	n/a
16	chr15:74365501-74365551	PANC-1	pancreas:	n/a
17	chr15:74357243-74357293	SAEC	small airway:	n/a
18	chr15:74365539-74365589	BE2_C	brain:	n/a
19	chr15:74392505-74392555	Hela-S3	cervix:	n/a
20	chr15:74357243-74357293	NH-A	brain:	n/a
21	chr15:74392505-74392555	HepG2	liver:	n/a
22	chr15:74392612-74392662	BJ	skin:	n/a
23	chr15:74392505-74392555	NHDF-neo	bronchial:	n/a
24	chr15:74365501-74365551	HEEpiC	esophagus:	n/a
25	chr15:74365501-74365551	T-47D	breast:	n/a
26	chr15:74365501-74365551	SK-N-SH_RA	brain:	n/a
27	chr15:74365539-74365589	HL-60	blood:	n/a
28	chr15:74357886-74357936	IMR90	lung:	fetal
29	chr15:74365101-74365151	Hela-S3	cervix:	n/a
30	chr15:74392505-74392555	GM19239	blood:	n/a
31	chr15:74392505-74392555	HPAEpiC	pulmonary alveolar:	n/a
32	chr15:74365501-74365551	AG09309	skin:	n/a
33	chr15:74392612-74392662	NT2-D1	testis:	n/a
34	chr15:74365539-74365589	HPAEpiC	pulmonary alveolar:	n/a
35	chr15:74392612-74392662	GM19239	blood:	n/a
36	chr15:74357886-74357936	NT2-D1	testis:	n/a
37	chr15:74357886-74357936	HCPEpiC	choroid plexus:	n/a
38	chr15:74365539-74365589	SK-N-MC	brain:	n/a
39	chr15:74365101-74365151	MCF-7	breast:	n/a
40	chr15:74357243-74357293	ProgFib	skin:	n/a
41	chr15:74357886-74357936	MCF-7	breast:	n/a
42	chr15:74396537-74396587	HRPEpiC	eye:	n/a
43	chr15:74357886-74357936	MCF10A-Er-Src	breast:	n/a
44	chr15:74365539-74365589	NB4	blood:	n/a
45	chr15:74365501-74365551	GM12878	blood:	n/a
46	chr15:74392612-74392662	SK-N-SH_RA	brain:	n/a
47	chr15:74365501-74365551	HMEC	breast:	n/a
48	chr15:74396537-74396587	AG04450	lung:	fetal
49	chr15:74396537-74396587	NHBE	bronchial:	n/a
50	chr15:74392505-74392555	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:74358127..74358835-chr15:74614868..74615479,2	MCF-7	breast:
2	chr15:74397359..74398863-chr15:76042857..76044553,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PML-2	chr15:74346640-74347125	XLOC_011309
2	lnc-RP11-247C2.2.1-2	chr15:74364764-74365039	NONHSAT047201
3	lnc-PML-2	chr15:74348320-74348558	XLOC_011309

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA6A	hsa-miR-192-5p	chr15:74362936-74362955

Variant related genes	Relation type
GOLGA6A	TF binding region
DNM1P33	TF binding region
RN7SL429P	TF binding region
ISLR2	TF binding region
ENSG00000214702	TF binding region
GOLGA6A	CpG island
DNM1P33	CpG island
RN7SL429P	CpG island
ISLR2	CpG island
ENSG00000214702	CpG island
MAN1A2	miRNA target sites
MAML1	miRNA target sites

Extended variants
information (count: 981 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:981 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189038095	chr15:74347120-74347121	Bivalent Enhancer Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
2	rs528657335	chr15:74347129-74347130	Bivalent Enhancer Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs28361371	chr15:74347140-74347141	Bivalent Enhancer Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs181476236	chr15:74347211-74347212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185705790	chr15:74347249-74347250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560545189	chr15:74347292-74347293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550513902	chr15:74347297-74347298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145515462	chr15:74347299-74347300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113898626	chr15:74347306-74347307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551442644	chr15:74347315-74347316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375624670	chr15:74347328-74347329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570651147	chr15:74347370-74347371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534487710	chr15:74347424-74347425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553245564	chr15:74347478-74347479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574600468	chr15:74347495-74347496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181936080	chr15:74347514-74347515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs8024467	chr15:74347518-74347519	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559831918	chr15:74347535-74347536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186128967	chr15:74347659-74347660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545943962	chr15:74347660-74347661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563999219	chr15:74347722-74347723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs8029133	chr15:74347723-74347724	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs540430774	chr15:74347836-74347837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562407626	chr15:74347842-74347843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143547426	chr15:74347844-74347845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189721776	chr15:74347916-74347917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1660013	chr15:74347917-74347918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1660012	chr15:74347919-74347920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562574565	chr15:74347943-74347944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1290342	chr15:74347971-74347972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533131942	chr15:74347975-74347976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138146629	chr15:74347988-74347989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559425817	chr15:74347994-74347995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181351368	chr15:74348021-74348022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1660011	chr15:74348036-74348037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs71399773	chr15:74348068-74348069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527733591	chr15:74348069-74348070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534646625	chr15:74348087-74348088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530039458	chr15:74348088-74348089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563266846	chr15:74348095-74348096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs71281947	chr15:74348098-74348099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534822085	chr15:74348106-74348107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546526395	chr15:74348110-74348111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528161135	chr15:74348131-74348132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542230521	chr15:74348152-74348153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs28572075	chr15:74348177-74348178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141892392	chr15:74348200-74348201	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185623917	chr15:74348220-74348221	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190772910	chr15:74348259-74348260	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183631054	chr15:74348275-74348276	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:195 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74342600-74365400	Weak transcription	Spleen	Spleen
2	chr15:74343400-74350400	Weak transcription	Left Ventricle	heart
3	chr15:74343400-74351200	Weak transcription	Aorta	Aorta
4	chr15:74343400-74358000	Weak transcription	Gastric	stomach
5	chr15:74343600-74347200	Enhancers	NHLF	lung
6	chr15:74344200-74350600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:74344600-74352400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:74346000-74347200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
9	chr15:74346000-74347200	Enhancers	Placenta	Placenta
10	chr15:74346200-74347200	Enhancers	Brain Angular Gyrus	brain
11	chr15:74346400-74347400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr15:74346800-74347200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
13	chr15:74346800-74347200	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr15:74346800-74347200	Enhancers	Osteobl	bone
15	chr15:74346800-74348000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:74346800-74348000	Weak transcription	K562	blood
17	chr15:74346800-74351400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr15:74346800-74351400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr15:74346800-74351600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr15:74346800-74351600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr15:74347000-74347200	Active TSS	A549	lung
22	chr15:74347000-74347400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:74347000-74348000	Weak transcription	Stomach Mucosa	stomach
24	chr15:74347000-74348000	Weak transcription	HMEC	breast
25	chr15:74347000-74348200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:74347000-74348200	Weak transcription	NHDF-Ad	bronchial
27	chr15:74347000-74349000	Enhancers	Hela-S3	cervix
28	chr15:74347000-74351400	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr15:74347000-74351800	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr15:74347200-74354000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr15:74348200-74348400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
32	chr15:74348200-74348400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr15:74348200-74348400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:74348200-74348400	Enhancers	Stomach Mucosa	stomach
35	chr15:74348200-74348400	Enhancers	HMEC	breast
36	chr15:74348200-74348400	Enhancers	HSMMtube	muscle
37	chr15:74348200-74348400	Enhancers	K562	blood
38	chr15:74348200-74349000	Enhancers	NHDF-Ad	bronchial
39	chr15:74351400-74352000	Enhancers	Primary T cells fromperipheralblood	blood
40	chr15:74351400-74352000	Enhancers	Thymus	Thymus
41	chr15:74351400-74352200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr15:74351400-74353200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr15:74351600-74352000	Enhancers	Primary T cells from cord blood	blood
44	chr15:74351600-74352000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr15:74351600-74352400	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr15:74351600-74352400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr15:74351800-74352400	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr15:74351800-74352400	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr15:74351800-74352400	Enhancers	Dnd41	blood
50	chr15:74352400-74352800	Weak transcription	Dnd41	blood

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