Variant report

Variant	nsv1025850
Chromosome Location	chr7:3446819-3474084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:3471268-3471422	HepG2	liver:	n/a	chr7:3471347-3471358
2	CEBPB	chr7:3471229-3471499	HepG2	liver:	n/a	chr7:3471347-3471358
3	CEBPB	chr7:3457543-3457997	H1-hESC	embryonic stem cell:	n/a	chr7:3457585-3457598 chr7:3457585-3457598
4	CTCF	chr7:3469703-3469748	MCF-7	breast:	n/a	n/a
5	CTCF	chr7:3470300-3470450	AG04449	skin:	n/a	n/a
6	CTCF	chr7:3471180-3471330	HA-sp	spinal cord:	n/a	n/a
7	CTCF	chr7:3471140-3471290	HAc	cerebellar:	n/a	n/a
8	CTCF	chr7:3470320-3470470	AG04449	skin:	n/a	n/a
9	CTCF	chr7:3470426-3470437	MCF-7	breast:	n/a	n/a
10	CTCF	chr7:3470400-3470550	AG04450	lung:	n/a	n/a
11	CTCF	chr7:3471260-3471410	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr7:3471260-3471410	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr7:3471260-3471410	HRE	kidney:	n/a	n/a
14	CTCF	chr7:3470380-3470530	Caco-2	colon:	n/a	n/a
15	CTCF	chr7:3465877-3465954	Fibrobl	skin:	n/a	n/a
16	CTCF	chr7:3470400-3470550	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr7:3470347-3470532	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr7:3470320-3470470	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr7:3470120-3470270	AG04450	lung:	n/a	n/a
20	CTCF	chr7:3470260-3470410	A549	lung:	n/a	n/a
21	CTCF	chr7:3470340-3470490	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr7:3470350-3470457	HepG2	liver:	n/a	n/a
23	CTCF	chr7:3470360-3470510	HPF	lung:	n/a	n/a
24	CTCF	chr7:3470340-3470490	HRE	kidney:	n/a	n/a
25	CTCF	chr7:3470300-3470450	NHEK	skin:	n/a	n/a
26	CTCF	chr7:3470380-3470530	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr7:3464411-3464473	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:3470392-3470490	NHEK	skin:	n/a	n/a
29	CTCF	chr7:3470272-3470574	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:3471240-3471390	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr7:3470320-3470470	HEK293	kidney:	n/a	n/a
32	CTCF	chr7:3470340-3470490	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:3470300-3470450	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr7:3470340-3470490	HAc	cerebellar:	n/a	n/a
35	EBF1	chr7:3448505-3448851	GM12878	blood:	n/a	n/a
36	EP300	chr7:3470050-3470610	MCF-7	breast:	n/a	n/a
37	FOS	chr7:3469813-3469845	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr7:3469778-3469815	MCF10A-Er-Src	breast:	n/a	n/a
39	GATA2	chr7:3464761-3464998	SH-SY5Y	brain:	n/a	chr7:3464869-3464878 chr7:3464922-3464931 chr7:3464921-3464931 chr7:3464922-3464929 chr7:3464920-3464932
40	GATA2	chr7:3450850-3451391	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr7:3470853-3471394	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr7:3470995-3471294	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr7:3455547-3456083	MCF-7	breast:	n/a	chr7:3455981-3455992
44	GATA3	chr7:3451000-3451444	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr7:3454813-3454894	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr7:3455504-3455704	SH-SY5Y	brain:	n/a	chr7:3455515-3455523
47	GATA3	chr7:3470881-3471541	SK-N-SH	brain:	n/a	n/a
48	GATA3	chr7:3464776-3465123	SH-SY5Y	brain:	n/a	chr7:3464869-3464878 chr7:3464922-3464931 chr7:3464921-3464931 chr7:3464922-3464929 chr7:3464920-3464932
49	KAP1	chr7:3465685-3466144	HEK293	kidney:	n/a	n/a
50	KAP1	chr7:3451864-3452928	HEK293	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3470434-3470484	PFSK-1	brain:	n/a
2	chr7:3470434-3470484	MCF10A-Er-Src	breast:	n/a
3	chr7:3470434-3470484	T-47D	breast:	n/a
4	chr7:3470434-3470484	HRPEpiC	eye:	n/a
5	chr7:3470434-3470484	AG04450	lung:	fetal
6	chr7:3470434-3470484	SK-N-MC	brain:	n/a
7	chr7:3470434-3470484	GM12891	blood:	n/a
8	chr7:3470434-3470484	SAEC	small airway:	n/a
9	chr7:3470434-3470484	GM06990	blood:	n/a
10	chr7:3470434-3470484	PANC-1	pancreas:	n/a
11	chr7:3470434-3470484	SK-N-SH_RA	brain:	n/a
12	chr7:3470434-3470484	HUVEC	blood vessel:	n/a
13	chr7:3470434-3470484	HL-60	blood:	n/a
14	chr7:3470434-3470484	AoSMC	blood vessel:	n/a
15	chr7:3470434-3470484	A549	lung:	n/a
16	chr7:3470434-3470484	SKMC	muscle:	n/a
17	chr7:3470434-3470484	NT2-D1	testis:	n/a
18	chr7:3470434-3470484	Hepatocyte	liver:	n/a
19	chr7:3470434-3470484	GM12892	blood:	n/a
20	chr7:3470434-3470484	HEEpiC	esophagus:	n/a
21	chr7:3470434-3470484	NHDF-neo	bronchial:	n/a
22	chr7:3470434-3470484	ProgFib	skin:	n/a
23	chr7:3470434-3470484	HCT-116	colon:	n/a
24	chr7:3470434-3470484	HRCEpiC	kidney:	n/a
25	chr7:3470434-3470484	NB4	blood:	n/a
26	chr7:3470434-3470484	PrEC	prostate:	n/a
27	chr7:3470434-3470484	BJ	skin:	n/a
28	chr7:3470434-3470484	AG09309	skin:	n/a
29	chr7:3470434-3470484	RPTEC	kidney:	n/a
30	chr7:3470434-3470484	GM19239	blood:	n/a
31	chr7:3470434-3470484	Hela-S3	cervix:	n/a
32	chr7:3470434-3470484	LNCaP	prostate:	n/a
33	chr7:3470434-3470484	U87	brain:	n/a
34	chr7:3470434-3470484	BE2_C	brain:	n/a
35	chr7:3470434-3470484	K562	blood:	n/a
36	chr7:3470434-3470484	H1-hESC	embryonic stem cell:	embryo
37	chr7:3470434-3470484	MCF-7	breast:	n/a
38	chr7:3470434-3470484	GM12878	blood:	n/a
39	chr7:3470434-3470484	SK-N-SH	brain:	n/a
40	chr7:3470434-3470484	Jurkat	blood:	n/a
41	chr7:3470434-3470484	NH-A	brain:	n/a
42	chr7:3470434-3470484	NHBE	bronchial:	n/a
43	chr7:3470434-3470484	HepG2	liver:	n/a
44	chr7:3470434-3470484	ovcar-3	ovarian:	n/a
45	chr7:3470434-3470484	HNPCEpiC	eye:	n/a
46	chr7:3470434-3470484	AG09319	gingival:	n/a
47	chr7:3470434-3470484	AG04449	skin:	fetal
48	chr7:3470434-3470484	IMR90	lung:	fetal
49	chr7:3470434-3470484	HCF	heart:	n/a
50	chr7:3470434-3470484	HAEpiC	amniotic membrane:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3450055..3452486-chr7:3794915..3797670,2	MCF-7	breast:
2	chr7:3466489..3468571-chr7:3470496..3474286,3	MCF-7	breast:
3	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
4	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
5	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
6	chr7:3442245..3445067-chr7:3448256..3450121,2	MCF-7	breast:
7	chr7:3466489..3468571-chr7:3470496..3474286,3	MCF-7	breast:
8	chr7:3438230..3440428-chr7:3448766..3450871,2	MCF-7	breast:
9	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
10	chr7:3467584..3469607-chr7:3473579..3476455,2	MCF-7	breast:
11	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
12	chr7:3240198..3242825-chr7:3445733..3447901,2	K562	blood:
13	chr7:3452987..3455737-chr7:3457417..3460056,3	MCF-7	breast:
14	chr7:3467584..3469607-chr7:3473579..3476455,2	MCF-7	breast:
15	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000211544	TF binding region
ENSG00000211544	CpG island
ENSG00000211544	chromatin interactions
ENSG00000146555	chromatin interactions

Extended variants
information (count: 1480 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17133277	chr7:3446819-3446820	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530561601	chr7:3446849-3446850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550648157	chr7:3446854-3446855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185500401	chr7:3446855-3446856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188808786	chr7:3446860-3446861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79302343	chr7:3446897-3446898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553324599	chr7:3446914-3446915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566724203	chr7:3446921-3446922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143270898	chr7:3446946-3446947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555312933	chr7:3446966-3446967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575389764	chr7:3447012-3447013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117043332	chr7:3447015-3447016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557409606	chr7:3447036-3447037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576841072	chr7:3447074-3447075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193037307	chr7:3447129-3447130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146686858	chr7:3447152-3447153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201219069	chr7:3447165-3447166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533559355	chr7:3447172-3447173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184611569	chr7:3447177-3447178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189168912	chr7:3447232-3447233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140242599	chr7:3447294-3447295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567788800	chr7:3447296-3447297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550439000	chr7:3447300-3447301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564174671	chr7:3447328-3447329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376013686	chr7:3447335-3447336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532960019	chr7:3447340-3447341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546577011	chr7:3447345-3447346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566466742	chr7:3447366-3447367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535794734	chr7:3447397-3447398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112787885	chr7:3447413-3447414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56064609	chr7:3447451-3447452	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs538009274	chr7:3447467-3447468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144880228	chr7:3447472-3447473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369776210	chr7:3447473-3447474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73298370	chr7:3447494-3447495	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs539460543	chr7:3447502-3447503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115776819	chr7:3447520-3447521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572899793	chr7:3447526-3447527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541426868	chr7:3447536-3447537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542186437	chr7:3447549-3447550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376713729	chr7:3447600-3447601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539722589	chr7:3447639-3447640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149123921	chr7:3447643-3447644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544744265	chr7:3447677-3447678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373492267	chr7:3447725-3447726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564034235	chr7:3447729-3447730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536706242	chr7:3447733-3447734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557725875	chr7:3447736-3447737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546713965	chr7:3447746-3447747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181196197	chr7:3447754-3447755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3437800-3448000	Weak transcription	Fetal Heart	heart
2	chr7:3443800-3450200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr7:3444400-3451800	Weak transcription	Fetal Brain Female	brain
4	chr7:3444800-3454800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:3445000-3448800	Weak transcription	NHEK	skin
6	chr7:3445200-3448400	Weak transcription	Fetal Brain Male	brain
7	chr7:3446200-3447000	Enhancers	Fetal Kidney	kidney
8	chr7:3446200-3447400	Weak transcription	Left Ventricle	heart
9	chr7:3446200-3449000	Weak transcription	Aorta	Aorta
10	chr7:3446400-3447000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:3446800-3447600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:3446800-3448400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:3446800-3448400	Weak transcription	Fetal Lung	lung
14	chr7:3447000-3447600	Enhancers	Pancreas	Pancrea
15	chr7:3447000-3457000	Weak transcription	Fetal Kidney	kidney
16	chr7:3447400-3447600	Enhancers	Left Ventricle	heart
17	chr7:3447600-3448600	Weak transcription	Left Ventricle	heart
18	chr7:3447600-3449000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:3447600-3450400	Weak transcription	Pancreas	Pancrea
20	chr7:3447800-3448000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:3448000-3449000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:3448000-3449000	Enhancers	Fetal Heart	heart
23	chr7:3448400-3448800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:3448400-3449000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:3448400-3449000	Enhancers	Brain Germinal Matrix	brain
26	chr7:3448400-3449200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:3448400-3449400	Enhancers	Fetal Brain Male	brain
28	chr7:3448400-3449400	Enhancers	Fetal Lung	lung
29	chr7:3448400-3449400	Enhancers	HSMMtube	muscle
30	chr7:3448400-3449600	Enhancers	Primary T cells from cord blood	blood
31	chr7:3448600-3448800	Enhancers	Adipose Nuclei	Adipose
32	chr7:3448600-3449200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:3448600-3449200	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr7:3448600-3449200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:3448600-3449400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:3448600-3449400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr7:3448600-3449400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr7:3448800-3449200	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr7:3448800-3449200	Enhancers	NHEK	skin
40	chr7:3449000-3449400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:3449000-3449400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr7:3449000-3449400	Enhancers	Primary T cells fromperipheralblood	blood
43	chr7:3449000-3449400	Enhancers	Aorta	Aorta
44	chr7:3449000-3449400	Enhancers	HSMM	muscle
45	chr7:3449200-3449400	Enhancers	Left Ventricle	heart
46	chr7:3449200-3450000	Weak transcription	NHEK	skin
47	chr7:3449400-3450400	Weak transcription	Fetal Brain Male	brain
48	chr7:3449400-3456200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:3449400-3456200	Weak transcription	Aorta	Aorta
50	chr7:3450000-3450600	Enhancers	Primary neutrophils fromperipheralblood	blood

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