Variant report

Variant	nsv1013388
Chromosome Location	chr4:69304927-69540013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1285)
CpG islands
(count:979)
Chromatin interactive
region (count:20)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
8	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
10	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
12	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
13	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
14	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
15	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
16	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
19	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
20	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
21	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
24	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
25	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
27	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
28	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
29	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
30	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
31	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
32	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
34	CEBPB	chr4:69312976-69313282	MCF-7	breast:	n/a	n/a
35	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
36	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
37	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
39	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
40	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
41	CEBPB	chr4:69308568-69308582	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
44	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
45	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
47	CTCF	chr4:69539000-69539150	GM12864	blood:	n/a	n/a
48	CTCF	chr4:69364180-69364461	GM12878	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
49	CTCF	chr4:69364168-69364470	A549	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
50	CTCF	chr4:69537340-69537490	HMEC	breast:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69537589-69537639	AG04450	lung:	fetal
2	chr4:69312104-69312154	HRPEpiC	eye:	n/a
3	chr4:69435250-69435300	HEEpiC	esophagus:	n/a
4	chr4:69537589-69537639	AG04450	lung:	fetal
5	chr4:69312104-69312154	HRPEpiC	eye:	n/a
6	chr4:69435250-69435300	HEEpiC	esophagus:	n/a
7	chr4:69355121-69355171	HRE	kidney:	n/a
8	chr4:69435250-69435300	BJ	skin:	n/a
9	chr4:69537806-69537856	HRPEpiC	eye:	n/a
10	chr4:69312104-69312154	HCF	heart:	n/a
11	chr4:69514031-69514081	GM19239	blood:	n/a
12	chr4:69340916-69340966	HCF	heart:	n/a
13	chr4:69514031-69514081	K562	blood:	n/a
14	chr4:69435601-69435651	HAEpiC	amniotic membrane:	n/a
15	chr4:69355121-69355171	GM12891	blood:	n/a
16	chr4:69536319-69536369	K562	blood:	n/a
17	chr4:69312104-69312154	NB4	blood:	n/a
18	chr4:69536319-69536369	HIPEpiC	eye:	n/a
19	chr4:69435250-69435300	HUVEC	blood vessel:	n/a
20	chr4:69536319-69536369	T-47D	breast:	n/a
21	chr4:69381368-69381418	HNPCEpiC	eye:	n/a
22	chr4:69536319-69536369	ProgFib	skin:	n/a
23	chr4:69340916-69340966	AG10803	skin:	n/a
24	chr4:69522639-69522689	Hela-S3	cervix:	n/a
25	chr4:69312514-69312564	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:69313197-69313247	HCT-116	colon:	n/a
27	chr4:69381368-69381418	U87	brain:	n/a
28	chr4:69537806-69537856	HRE	kidney:	n/a
29	chr4:69435601-69435651	LNCaP	prostate:	n/a
30	chr4:69435593-69435643	AG09319	gingival:	n/a
31	chr4:69537589-69537639	GM12891	blood:	n/a
32	chr4:69434475-69434525	H1-hESC	embryonic stem cell:	embryo
33	chr4:69536319-69536369	U87	brain:	n/a
34	chr4:69537806-69537856	HEEpiC	esophagus:	n/a
35	chr4:69514031-69514081	H1-hESC	embryonic stem cell:	embryo
36	chr4:69435601-69435651	K562	blood:	n/a
37	chr4:69537806-69537856	CMK	blood:	n/a
38	chr4:69434475-69434525	Caco-2	colon:	n/a
39	chr4:69537589-69537639	HCM	heart:	n/a
40	chr4:69434475-69434525	SKMC	muscle:	n/a
41	chr4:69355121-69355171	NT2-D1	testis:	n/a
42	chr4:69434475-69434525	Hela-S3	cervix:	n/a
43	chr4:69435593-69435643	LNCaP	prostate:	n/a
44	chr4:69537806-69537856	SK-N-MC	brain:	n/a
45	chr4:69355121-69355171	RPTEC	kidney:	n/a
46	chr4:69537826-69537876	GM12878	blood:	n/a
47	chr4:69537826-69537876	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:69537806-69537856	NT2-D1	testis:	n/a
49	chr4:69340916-69340966	H1-hESC	embryonic stem cell:	embryo
50	chr4:69435601-69435651	HMEC	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
2	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
3	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
4	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
5	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
6	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
7	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
8	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
9	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
10	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
11	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
12	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
13	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
14	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
15	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
16	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
17	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
18	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
19	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
20	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
2	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
3	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
4	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
5	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
6	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
TMPRSS11E	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
TMPRSS11E	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000249985	chromatin interactions
ENSG00000087128	chromatin interactions
ENSG00000083896	chromatin interactions
ENSG00000272626	chromatin interactions

Extended variants
information (count: 7074 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:7074 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550983145	chr4:69304930-69304931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570851839	chr4:69304936-69304937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539960558	chr4:69305089-69305090	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs187435213	chr4:69305218-69305219	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs4272079	chr4:69305317-69305318	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs369856614	chr4:69305319-69305320	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs374667278	chr4:69305378-69305379	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs71615089	chr4:69305379-69305380	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs62317528	chr4:69305462-69305463	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs139048807	chr4:69305537-69305538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs67593708	chr4:69305538-69305539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs71218975	chr4:69305540-69305541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376045932	chr4:69305541-69305542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369426261	chr4:69305551-69305552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367789262	chr4:69305556-69305557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531524304	chr4:69305573-69305574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374358566	chr4:69305574-69305575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540326420	chr4:69305582-69305583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551923550	chr4:69305616-69305617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192025435	chr4:69305622-69305623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571677305	chr4:69305647-69305648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562024841	chr4:69305725-69305726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376412568	chr4:69305726-69305727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544269230	chr4:69305751-69305752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564512372	chr4:69305757-69305758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs62317529	chr4:69305762-69305763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567545981	chr4:69305767-69305768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547138178	chr4:69305768-69305769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145193463	chr4:69305770-69305771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553231447	chr4:69305787-69305788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35805944	chr4:69305799-69305800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs549225989	chr4:69305849-69305850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554489124	chr4:69305853-69305854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183784964	chr4:69305870-69305871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142448396	chr4:69305923-69305924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557421463	chr4:69305998-69305999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189248242	chr4:69306010-69306011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs151307258	chr4:69306133-69306134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565655032	chr4:69306138-69306139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553438054	chr4:69306151-69306152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573431447	chr4:69306159-69306160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141720498	chr4:69306221-69306222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555579878	chr4:69306296-69306297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1406697	chr4:69306340-69306341	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs62317530	chr4:69306350-69306351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13115399	chr4:69306355-69306356	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs564292329	chr4:69306356-69306357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141126008	chr4:69306359-69306360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1406698	chr4:69306403-69306404	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs560546123	chr4:69306409-69306410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69296600-69312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:69301000-69305800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:69301800-69307400	Enhancers	Primary B cells from peripheral blood	blood
4	chr4:69302800-69312000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:69303400-69305600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr4:69304600-69305000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr4:69304600-69306600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:69304600-69306800	Enhancers	Primary T cells fromperipheralblood	blood
9	chr4:69304600-69307200	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr4:69304600-69307400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr4:69304600-69307400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr4:69304600-69308400	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr4:69304600-69308400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr4:69304600-69308400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr4:69304800-69305600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:69304800-69305600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:69304800-69305600	Enhancers	Fetal Thymus	thymus
18	chr4:69304800-69305600	Enhancers	Dnd41	blood
19	chr4:69304800-69306200	Enhancers	Primary hematopoietic stem cells	blood
20	chr4:69304800-69307400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr4:69304800-69308000	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr4:69304800-69308600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr4:69304800-69310000	Enhancers	Primary T cells from cord blood	blood
24	chr4:69305000-69305400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
25	chr4:69305400-69307000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr4:69305600-69306800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr4:69307200-69309200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr4:69307400-69308400	Weak transcription	Primary B cells from peripheral blood	blood
29	chr4:69307400-69310400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr4:69308400-69308600	Enhancers	Primary B cells from peripheral blood	blood
31	chr4:69308400-69317800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr4:69309200-69309600	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr4:69310000-69314000	Weak transcription	Primary T cells from cord blood	blood
34	chr4:69310400-69310600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr4:69310400-69310600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr4:69310400-69311000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr4:69310600-69310800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr4:69310600-69310800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr4:69310600-69312000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr4:69310800-69312200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr4:69311000-69312000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr4:69311200-69311400	Enhancers	HMEC	breast
43	chr4:69311600-69312800	Weak transcription	HMEC	breast
44	chr4:69311800-69321200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:69312000-69312200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:69312000-69312200	Enhancers	H9 Cell Line	embryonic stem cell
47	chr4:69312000-69312600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:69312000-69312800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr4:69312000-69312800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:69312000-69313200	Enhancers	H1 Cell Line	embryonic stem cell

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