Variant report

Variant	nsv471505
Chromosome Location	chr7:102114386-102418049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8512)
CpG islands
(count:2752)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:8512 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102212897-102213097	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102339769-102340073	K562	blood:	n/a	n/a
3	ARID3A	chr7:102386072-102386189	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:102386048-102386259	K562	blood:	n/a	n/a
5	ARID3A	chr7:102389084-102389458	HepG2	liver:	n/a	n/a
6	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
7	ATF1	chr7:102389031-102389497	K562	blood:	n/a	n/a
8	ATF2	chr7:102389108-102389584	GM12878	blood:	n/a	n/a
9	ATF2	chr7:102353714-102354151	GM12878	blood:	n/a	n/a
10	ATF2	chr7:102153014-102153393	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:102389081-102389544	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:102353660-102354116	GM12878	blood:	n/a	n/a
13	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
14	ATF3	chr7:102213014-102213141	GM12878	blood:	n/a	n/a
15	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
16	ATF3	chr7:102213014-102213188	K562	blood:	n/a	n/a
17	BACH1	chr7:102213021-102213172	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr7:102234392-102234834	GM12878	blood:	n/a	n/a
19	BATF	chr7:102118716-102119971	GM12878	blood:	n/a	n/a
20	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
21	BATF	chr7:102212379-102213628	GM12878	blood:	n/a	n/a
22	BATF	chr7:102187719-102187949	GM12878	blood:	n/a	n/a
23	BATF	chr7:102356182-102356563	GM12878	blood:	n/a	n/a
24	BATF	chr7:102117408-102117666	GM12878	blood:	n/a	n/a
25	BATF	chr7:102117804-102118098	GM12878	blood:	n/a	n/a
26	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
27	BATF	chr7:102179720-102179981	GM12878	blood:	n/a	n/a
28	BATF	chr7:102353557-102354555	GM12878	blood:	n/a	n/a
29	BATF	chr7:102207398-102207660	GM12878	blood:	n/a	n/a
30	BATF	chr7:102205933-102206440	GM12878	blood:	n/a	n/a
31	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
32	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
33	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
34	BATF	chr7:102192870-102193124	GM12878	blood:	n/a	n/a
35	BATF	chr7:102355536-102355847	GM12878	blood:	n/a	n/a
36	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
37	BATF	chr7:102192070-102192285	GM12878	blood:	n/a	n/a
38	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
39	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
40	BATF	chr7:102256202-102256653	GM12878	blood:	n/a	n/a
41	BATF	chr7:102185674-102186087	GM12878	blood:	n/a	n/a
42	BATF	chr7:102185510-102186196	GM12878	blood:	n/a	n/a
43	BATF	chr7:102247244-102247556	GM12878	blood:	n/a	n/a
44	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
45	BATF	chr7:102155139-102156246	GM12878	blood:	n/a	n/a
46	BATF	chr7:102212695-102213163	GM12878	blood:	n/a	n/a
47	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
48	BATF	chr7:102214085-102214343	GM12878	blood:	n/a	n/a
49	BATF	chr7:102134745-102135058	GM12878	blood:	n/a	n/a
50	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a

(count:2752 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102196182-102196232	AoSMC	blood vessel:	n/a
2	chr7:102132012-102132062	NH-A	brain:	n/a
3	chr7:102279588-102279638	HCPEpiC	choroid plexus:	n/a
4	chr7:102389275-102389325	SK-N-SH_RA	brain:	n/a
5	chr7:102119729-102119779	HCM	heart:	n/a
6	chr7:102389327-102389377	A549	lung:	n/a
7	chr7:102312308-102312358	HRPEpiC	eye:	n/a
8	chr7:102196182-102196232	AoSMC	blood vessel:	n/a
9	chr7:102132012-102132062	NH-A	brain:	n/a
10	chr7:102279588-102279638	HCPEpiC	choroid plexus:	n/a
11	chr7:102389275-102389325	SK-N-SH_RA	brain:	n/a
12	chr7:102119729-102119779	HCM	heart:	n/a
13	chr7:102389327-102389377	A549	lung:	n/a
14	chr7:102312308-102312358	HRPEpiC	eye:	n/a
15	chr7:102385712-102385762	SK-N-MC	brain:	n/a
16	chr7:102118300-102118350	PFSK-1	brain:	n/a
17	chr7:102136524-102136574	Hepatocyte	liver:	n/a
18	chr7:102389790-102389840	HL-60	blood:	n/a
19	chr7:102389191-102389241	ECC-1	luminal epithelium:	n/a
20	chr7:102389481-102389531	BJ	skin:	n/a
21	chr7:102161506-102161556	Jurkat	blood:	n/a
22	chr7:102389481-102389531	NHDF-neo	bronchial:	n/a
23	chr7:102329146-102329196	LNCaP	prostate:	n/a
24	chr7:102136524-102136574	Caco-2	colon:	n/a
25	chr7:102389205-102389255	Hepatocyte	liver:	n/a
26	chr7:102389205-102389255	HL-60	blood:	n/a
27	chr7:102332458-102332508	H1-hESC	embryonic stem cell:	embryo
28	chr7:102389892-102389942	HRE	kidney:	n/a
29	chr7:102196182-102196232	NT2-D1	testis:	n/a
30	chr7:102312308-102312358	HRCEpiC	kidney:	n/a
31	chr7:102311965-102312015	T-47D	breast:	n/a
32	chr7:102389790-102389840	HMEC	breast:	n/a
33	chr7:102155527-102155577	AG09309	skin:	n/a
34	chr7:102119529-102119579	ovcar-3	ovarian:	n/a
35	chr7:102330635-102330685	CMK	blood:	n/a
36	chr7:102136524-102136574	SAEC	small airway:	n/a
37	chr7:102389892-102389942	AG10803	skin:	n/a
38	chr7:102389315-102389365	HEK293	kidney:	embryo
39	chr7:102312200-102312250	NHDF-neo	bronchial:	n/a
40	chr7:102212892-102212942	AoSMC	blood vessel:	n/a
41	chr7:102329146-102329196	SK-N-SH	brain:	n/a
42	chr7:102389892-102389942	HMEC	breast:	n/a
43	chr7:102389239-102389289	LNCaP	prostate:	n/a
44	chr7:102389239-102389289	K562	blood:	n/a
45	chr7:102389315-102389365	H1-hESC	embryonic stem cell:	embryo
46	chr7:102327236-102327286	NT2-D1	testis:	n/a
47	chr7:102259241-102259291	GM06990	blood:	n/a
48	chr7:102385712-102385762	T-47D	breast:	n/a
49	chr7:102329146-102329196	Hela-S3	cervix:	n/a
50	chr7:102122352-102122402	PFSK-1	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102388357..102390801-chr7:102713734..102717426,3	K562	blood:
2	chr7:76751236..76752770-chr7:102389322..102390934,2	MCF-7	breast:
3	chr7:102389047..102390959-chr7:102788572..102791008,2	K562	blood:
4	chr7:76751236..76751872-chr7:102389110..102389768,2	MCF-7	breast:
5	chr7:76750772..76751740-chr7:102389401..102390157,2	HCT-116	colon:
6	chr7:102387955..102390990-chr7:102714406..102717094,4	MCF-7	breast:
7	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:
8	chr7:102396782..102398459-chr7:102714684..102716364,2	MCF-7	breast:
9	chr7:102389494..102391981-chr7:102714130..102716680,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR2J-1	chr7:102120179-102121095	NONHSAT122510

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RASA4	hsa-miR-335-5p	chr7:102227581-102227605
2	RASA4	hsa-miR-335-5p	chr7:102128407-102128431

Variant related genes	Relation type
ENSG00000270249	TF binding region
RASA4B	TF binding region
ENSG00000272949	TF binding region
ENSG00000205236	TF binding region
POLR2J	TF binding region
ENSG00000228049	TF binding region
ENSG00000238997	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
ENSG00000213385	TF binding region
SPDYE2	TF binding region
ENSG00000271745	TF binding region
RASA4	TF binding region
RASA4DP	TF binding region
FAM185A	TF binding region
POLR2J3	TF binding region
SPDYE2B	TF binding region
ENSG00000256604	TF binding region
ENSG00000238392	TF binding region
ENSG00000270249	CpG island
RASA4B	CpG island
ENSG00000272949	CpG island
ENSG00000205236	CpG island
POLR2J	CpG island
ENSG00000228049	CpG island
ENSG00000238997	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
ENSG00000213385	CpG island
SPDYE2	CpG island
ENSG00000271745	CpG island
RASA4	CpG island
RASA4DP	CpG island
FAM185A	CpG island
POLR2J3	CpG island
SPDYE2B	CpG island
ENSG00000256604	CpG island
ENSG00000238392	CpG island
ENSG00000161040	chromatin interactions
ENSG00000161048	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000264471	chromatin interactions
ENSG00000135205	chromatin interactions
ENSG00000214439	chromatin interactions

Extended variants
information (count: 3986 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3986 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187474922	chr7:102114405-102114406	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559217120	chr7:102114410-102114411	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577481090	chr7:102114413-102114414	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9692124	chr7:102114424-102114425	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559141556	chr7:102114426-102114427	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574475137	chr7:102114437-102114438	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142762939	chr7:102114441-102114442	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs563269365	chr7:102114447-102114448	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35002684	chr7:102114453-102114454	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112691470	chr7:102114455-102114456	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34808331	chr7:102114456-102114457	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563946887	chr7:102114458-102114459	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555640783	chr7:102114464-102114465	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111541552	chr7:102114465-102114466	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573748878	chr7:102114475-102114476	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546386126	chr7:102114481-102114482	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566081651	chr7:102114490-102114491	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115839223	chr7:102114498-102114499	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs548321284	chr7:102114501-102114502	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570005795	chr7:102114503-102114504	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192020940	chr7:102114507-102114508	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116733631	chr7:102114508-102114509	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
23	rs571061099	chr7:102114513-102114514	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535283947	chr7:102114517-102114518	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560256718	chr7:102114518-102114519	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572417991	chr7:102114543-102114544	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574473632	chr7:102114547-102114548	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9691416	chr7:102114556-102114557	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556696175	chr7:102114575-102114576	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574851774	chr7:102114617-102114618	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62483808	chr7:102114631-102114632	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs564086025	chr7:102114661-102114662	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528359333	chr7:102114697-102114698	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540089468	chr7:102114700-102114701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561899337	chr7:102114703-102114704	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530158578	chr7:102114720-102114721	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs56296803	chr7:102114749-102114750	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201181784	chr7:102114750-102114751	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530882035	chr7:102114758-102114759	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552604223	chr7:102114766-102114767	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571205876	chr7:102114780-102114781	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375512750	chr7:102114800-102114801	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11157	chr7:102114819-102114820	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368336877	chr7:102114834-102114835	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148023737	chr7:102114838-102114839	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200167532	chr7:102114850-102114851	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142554831	chr7:102114858-102114859	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535205226	chr7:102114907-102114908	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556969085	chr7:102114964-102114965	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527641008	chr7:102114989-102114990	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2083 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102106400-102119400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:102106600-102115000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:102106600-102119200	Weak transcription	Right Atrium	heart
4	chr7:102106800-102114400	Weak transcription	Brain Angular Gyrus	brain
5	chr7:102106800-102114400	Strong transcription	NHLF	lung
6	chr7:102106800-102114600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:102106800-102114600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:102106800-102116400	Strong transcription	Fetal Stomach	stomach
9	chr7:102106800-102118800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:102106800-102119200	Weak transcription	NHDF-Ad	bronchial
11	chr7:102107400-102116200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:102107400-102116200	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:102107600-102118200	Weak transcription	HUVEC	blood vessel
14	chr7:102107600-102119200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:102107600-102120400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr7:102107800-102114400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:102107800-102114400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:102107800-102114600	Strong transcription	Primary B cells from peripheral blood	blood
19	chr7:102107800-102114600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:102107800-102114800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:102107800-102115600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr7:102107800-102116000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:102107800-102116400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr7:102107800-102118000	Weak transcription	NH-A	brain
25	chr7:102108000-102114600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:102108000-102114600	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr7:102108000-102114600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:102108000-102114600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr7:102108000-102114600	Strong transcription	Fetal Brain Female	brain
30	chr7:102108000-102114800	Strong transcription	Thymus	Thymus
31	chr7:102108000-102115000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr7:102108000-102115400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr7:102108000-102115600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:102108200-102115000	Strong transcription	Fetal Thymus	thymus
35	chr7:102108600-102114600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr7:102108800-102114800	Strong transcription	Brain Germinal Matrix	brain
37	chr7:102109000-102114400	Strong transcription	Esophagus	oesophagus
38	chr7:102109000-102114400	Strong transcription	Fetal Intestine Large	intestine
39	chr7:102109800-102114600	Strong transcription	Right Ventricle	heart
40	chr7:102110000-102114400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:102110600-102114400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:102110600-102118200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:102111000-102114800	Strong transcription	Gastric	stomach
44	chr7:102111000-102114800	Strong transcription	Spleen	Spleen
45	chr7:102111000-102116400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr7:102111000-102116400	Strong transcription	Fetal Intestine Small	intestine
47	chr7:102111600-102114600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr7:102111600-102115000	Strong transcription	Lung	lung
49	chr7:102111800-102114600	Strong transcription	Osteobl	bone
50	chr7:102112000-102114400	Strong transcription	Primary T helper cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links