Variant report

Variant	esv3584544
Chromosome Location	chr7:3107079-3127923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:3106942-3107186	K562	blood:	n/a	n/a
2	ATF2	chr7:3108146-3108703	GM12878	blood:	n/a	n/a
3	ATF2	chr7:3108148-3108734	GM12878	blood:	n/a	n/a
4	ATF2	chr7:3118056-3118550	GM12878	blood:	n/a	n/a
5	ATF2	chr7:3106806-3107600	GM12878	blood:	n/a	n/a
6	ATF2	chr7:3106829-3107344	GM12878	blood:	n/a	n/a
7	ATF2	chr7:3118024-3118508	GM12878	blood:	n/a	n/a
8	ATF3	chr7:3106922-3107172	GM12878	blood:	n/a	n/a
9	BATF	chr7:3108295-3108545	GM12878	blood:	n/a	n/a
10	BATF	chr7:3114599-3114890	GM12878	blood:	n/a	n/a
11	BATF	chr7:3118166-3118517	GM12878	blood:	n/a	n/a
12	BATF	chr7:3107333-3107645	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:3108184-3108629	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:3118127-3118458	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:3118124-3118494	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:3108267-3108567	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:3106940-3107212	K562	blood:	n/a	n/a
18	BHLHE40	chr7:3118138-3118639	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:3106998-3107263	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:3107943-3107999	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:3126085-3126131	K562	blood:	n/a	n/a
22	BHLHE40	chr7:3122367-3122715	K562	blood:	n/a	chr7:3122437-3122446
23	BHLHE40	chr7:3120025-3120105	K562	blood:	n/a	n/a
24	BHLHE40	chr7:3118443-3118622	K562	blood:	n/a	n/a
25	BHLHE40	chr7:3108257-3108558	GM12878	blood:	n/a	n/a
26	CEBPB	chr7:3115199-3115474	IMR90	lung:	n/a	chr7:3115311-3115322
27	CEBPB	chr7:3115188-3115472	Hela-S3	cervix:	n/a	chr7:3115311-3115322
28	CEBPB	chr7:3108155-3108486	HepG2	liver:	n/a	chr7:3108298-3108309
29	CEBPB	chr7:3115156-3115502	HepG2	liver:	n/a	chr7:3115311-3115322
30	CEBPB	chr7:3109688-3110110	MCF-7	breast:	n/a	chr7:3109883-3109894
31	CEBPB	chr7:3115189-3115491	K562	blood:	n/a	chr7:3115311-3115322
32	CEBPB	chr7:3108232-3108401	H1-hESC	embryonic stem cell:	n/a	chr7:3108298-3108309
33	CEBPB	chr7:3109807-3110007	Hela-S3	cervix:	n/a	chr7:3109883-3109894
34	CEBPB	chr7:3109745-3110027	H1-hESC	embryonic stem cell:	n/a	chr7:3109883-3109894
35	CEBPB	chr7:3108263-3108392	K562	blood:	n/a	chr7:3108298-3108309
36	CEBPB	chr7:3109775-3110077	K562	blood:	n/a	chr7:3109883-3109894
37	CEBPB	chr7:3108191-3108463	Hela-S3	cervix:	n/a	chr7:3108298-3108309
38	CEBPB	chr7:3109700-3110064	A549	lung:	n/a	chr7:3109883-3109894
39	CEBPB	chr7:3109705-3110068	HepG2	liver:	n/a	chr7:3109883-3109894
40	CEBPB	chr7:3116404-3116590	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:3108154-3108481	A549	lung:	n/a	chr7:3108298-3108309
42	CEBPB	chr7:3108165-3108448	IMR90	lung:	n/a	chr7:3108298-3108309
43	CEBPB	chr7:3108052-3108967	GM12878	blood:	n/a	chr7:3108298-3108309
44	CEBPB	chr7:3115180-3115481	A549	lung:	n/a	chr7:3115311-3115322
45	CEBPB	chr7:3109736-3110058	IMR90	lung:	n/a	chr7:3109883-3109894
46	CEBPB	chr7:3116334-3116728	HepG2	liver:	n/a	n/a
47	CHD2	chr7:3117626-3117667	HepG2	liver:	n/a	n/a
48	CHD2	chr7:3118168-3118456	GM12878	blood:	n/a	n/a
49	CREB1	chr7:3118037-3118644	GM12878	blood:	n/a	n/a
50	CREB1	chr7:3106805-3107385	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3127028-3127078	HCT-116	colon:	n/a
2	chr7:3127028-3127078	PrEC	prostate:	n/a
3	chr7:3127028-3127078	AG04450	lung:	fetal
4	chr7:3127028-3127078	K562	blood:	n/a
5	chr7:3127028-3127078	IMR90	lung:	fetal
6	chr7:3127028-3127078	HMEC	breast:	n/a
7	chr7:3127028-3127078	HUVEC	blood vessel:	n/a
8	chr7:3127028-3127078	HRPEpiC	eye:	n/a
9	chr7:3127028-3127078	Hela-S3	cervix:	n/a
10	chr7:3127028-3127078	BJ	skin:	n/a
11	chr7:3127028-3127078	NT2-D1	testis:	n/a
12	chr7:3127028-3127078	SK-N-SH	brain:	n/a
13	chr7:3127028-3127078	BE2_C	brain:	n/a
14	chr7:3127028-3127078	NH-A	brain:	n/a
15	chr7:3127028-3127078	GM06990	blood:	n/a
16	chr7:3127028-3127078	SKMC	muscle:	n/a
17	chr7:3127028-3127078	HEK293	kidney:	embryo
18	chr7:3127028-3127078	Caco-2	colon:	n/a
19	chr7:3127028-3127078	GM12892	blood:	n/a
20	chr7:3127028-3127078	HNPCEpiC	eye:	n/a
21	chr7:3127028-3127078	SK-N-SH_RA	brain:	n/a
22	chr7:3127028-3127078	HRE	kidney:	n/a
23	chr7:3127028-3127078	AoSMC	blood vessel:	n/a
24	chr7:3127028-3127078	Jurkat	blood:	n/a
25	chr7:3127028-3127078	GM12891	blood:	n/a
26	chr7:3127028-3127078	HIPEpiC	eye:	n/a
27	chr7:3127028-3127078	AG09319	gingival:	n/a
28	chr7:3127028-3127078	SK-N-MC	brain:	n/a
29	chr7:3127028-3127078	AG04449	skin:	fetal
30	chr7:3127028-3127078	ProgFib	skin:	n/a
31	chr7:3127028-3127078	NB4	blood:	n/a
32	chr7:3127028-3127078	GM19239	blood:	n/a
33	chr7:3127028-3127078	GM12878	blood:	n/a
34	chr7:3127028-3127078	PANC-1	pancreas:	n/a
35	chr7:3127028-3127078	MCF10A-Er-Src	breast:	n/a
36	chr7:3127028-3127078	PFSK-1	brain:	n/a
37	chr7:3127028-3127078	HRCEpiC	kidney:	n/a
38	chr7:3127028-3127078	AG09309	skin:	n/a
39	chr7:3127028-3127078	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:3127028-3127078	LNCaP	prostate:	n/a
41	chr7:3127028-3127078	NHDF-neo	bronchial:	n/a
42	chr7:3127028-3127078	A549	lung:	n/a
43	chr7:3127028-3127078	ovcar-3	ovarian:	n/a
44	chr7:3127028-3127078	AG10803	skin:	n/a
45	chr7:3127028-3127078	HL-60	blood:	n/a
46	chr7:3127028-3127078	MCF-7	breast:	n/a
47	chr7:3127028-3127078	HAEpiC	amniotic membrane:	n/a
48	chr7:3127028-3127078	HEEpiC	esophagus:	n/a
49	chr7:3127028-3127078	CMK	blood:	n/a
50	chr7:3127028-3127078	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:2913908..2916162-chr7:3122594..3124369,2	MCF-7	breast:
2	chr7:2913414..2914953-chr7:3113951..3116529,2	MCF-7	breast:
3	chr7:3113104..3115838-chr7:3115974..3117943,2	K562	blood:
4	chr7:3113104..3115838-chr7:3115974..3117943,2	K562	blood:
5	chr7:3114729..3116313-chr7:3116448..3118369,2	MCF-7	breast:
6	chr7:3095854..3098003-chr7:3113268..3116037,2	K562	blood:
7	chr7:3102265..3103829-chr7:3107588..3109384,2	MCF-7	breast:
8	chr7:3114729..3116313-chr7:3116448..3118369,2	MCF-7	breast:
9	chr7:2926330..2927157-chr7:3107129..3108063,2	K562	blood:
10	chr17:56735316..56738174-chr7:3105688..3107958,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD11-3	chr7:3124135-3124176	l_3354_chr7:3100290-3107234_whiteBloodCell
2	lnc-CARD11-1	chr7:3125986-3126055	XLOC_006337
3	lnc-CARD11-1	chr7:3122886-3123252	XLOC_006337
4	lnc-CARD11-3	chr7:3107182-3107234	l_3354_chr7:3100290-3107234_whiteBloodCell

No data

Variant related genes	Relation type
ENSG00000228334	TF binding region
ENSG00000228334	CpG island
ENSG00000202077	chromatin interactions

Extended variants
information (count: 975 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:975 , 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	rs6942522	chr7:3107079-3107080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527987162	chr7:3107084-3107085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143188658	chr7:3107092-3107093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550414203	chr7:3107110-3107111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560744120	chr7:3107165-3107166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs4722382	chr7:3107183-3107184	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549647417	chr7:3107184-3107185	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs569761809	chr7:3107195-3107196	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs532397394	chr7:3107216-3107217	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs34671447	chr7:3107224-3107225	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs529962865	chr7:3107268-3107269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188636798	chr7:3107286-3107287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566799587	chr7:3107294-3107295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565842728	chr7:3107325-3107326	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs193237076	chr7:3107333-3107334	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534100452	chr7:3107381-3107382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532233946	chr7:3107384-3107385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548440745	chr7:3107397-3107398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148260096	chr7:3107446-3107447	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536640001	chr7:3107461-3107462	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs78887508	chr7:3107558-3107559	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs79818515	chr7:3107601-3107602	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571782026	chr7:3107614-3107615	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558743984	chr7:3107617-3107618	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs141437847	chr7:3107708-3107709	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75135960	chr7:3107710-3107711	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571560543	chr7:3107735-3107736	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138100501	chr7:3107747-3107748	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143142969	chr7:3107775-3107776	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185017944	chr7:3107802-3107803	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543440788	chr7:3107803-3107804	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377610116	chr7:3107844-3107845	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563229885	chr7:3107908-3107909	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149979860	chr7:3107909-3107910	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369072722	chr7:3107911-3107912	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200357494	chr7:3107913-3107914	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532258482	chr7:3107924-3107925	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532688843	chr7:3107935-3107936	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575682625	chr7:3107968-3107969	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs150844017	chr7:3107977-3107978	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs559309009	chr7:3107993-3107994	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs189053375	chr7:3108001-3108002	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs138158465	chr7:3108033-3108034	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs181722583	chr7:3108074-3108075	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs34731274	chr7:3108079-3108080	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs536899685	chr7:3108113-3108114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs549771994	chr7:3108127-3108128	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs149552039	chr7:3108199-3108200	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs542845924	chr7:3108209-3108210	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs79344448	chr7:3108225-3108226	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3102000-3113800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr7:3102600-3109800	Enhancers	Primary B cells from cord blood	blood
3	chr7:3103000-3107400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:3103200-3108600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
5	chr7:3103200-3110200	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr7:3103200-3110400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr7:3103200-3110400	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr7:3103200-3110800	Enhancers	Primary T cells fromperipheralblood	blood
9	chr7:3103200-3111000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr7:3103400-3108800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr7:3103400-3109200	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr7:3103400-3109600	Enhancers	GM12878-XiMat	blood
13	chr7:3104800-3109800	Enhancers	Primary B cells from peripheral blood	blood
14	chr7:3105400-3109200	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr7:3105600-3107800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:3105800-3109200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr7:3105800-3109400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:3105800-3109400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr7:3105800-3113600	Weak transcription	Aorta	Aorta
20	chr7:3106000-3108000	Weak transcription	Fetal Thymus	thymus
21	chr7:3106400-3110000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:3106600-3108000	Weak transcription	Primary T cells from cord blood	blood
23	chr7:3106800-3108400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr7:3107000-3110200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:3107400-3108400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
26	chr7:3107600-3110000	Enhancers	Primary hematopoietic stem cells	blood
27	chr7:3107800-3108200	Enhancers	Duodenum Mucosa	Duodenum
28	chr7:3107800-3108800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr7:3107800-3110000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:3108000-3108200	Enhancers	Fetal Thymus	thymus
31	chr7:3108000-3109200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:3108000-3110000	Enhancers	Primary T cells from cord blood	blood
33	chr7:3108200-3108600	Weak transcription	Fetal Thymus	thymus
34	chr7:3108400-3110400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:3108600-3109800	Enhancers	Fetal Thymus	thymus
36	chr7:3108800-3109000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:3108800-3109200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr7:3108800-3111600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:3109000-3109400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr7:3109000-3110000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr7:3109200-3109800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr7:3109200-3109800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
43	chr7:3109200-3109800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:3109200-3110000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr7:3109400-3109600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr7:3109400-3109800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr7:3109400-3109800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr7:3109400-3109800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr7:3109400-3109800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:3109800-3110200	Enhancers	Primary T helper cells PMA-I stimulated	--

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