Variant report

Variant	esv274999
Chromosome Location	chr7:150701010-150708089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:657)
CpG islands
(count:734)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150707551-150707746	K562	blood:	n/a	n/a
2	ARID3A	chr7:150702885-150703054	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:150705096-150706111	K562	blood:	n/a	n/a
4	ATF1	chr7:150705143-150706133	K562	blood:	n/a	n/a
5	ATF2	chr7:150705746-150706227	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr7:150700595-150701087	K562	blood:	n/a	n/a
7	ATF3	chr7:150706455-150706881	K562	blood:	n/a	n/a
8	BACH1	chr7:150705380-150706071	K562	blood:	n/a	n/a
9	BACH1	chr7:150705850-150706094	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:150707503-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:150707629-150707768	K562	blood:	n/a	n/a
12	BCLAF1	chr7:150705267-150706200	K562	blood:	n/a	n/a
13	BHLHE40	chr7:150700538-150701020	K562	blood:	n/a	n/a
14	BHLHE40	chr7:150707405-150708222	K562	blood:	n/a	n/a
15	BHLHE40	chr7:150705759-150706350	HepG2	liver:	n/a	n/a
16	BHLHE40	chr7:150700651-150701010	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:150705569-150706124	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:150705149-150706877	K562	blood:	n/a	n/a
19	BRCA1	chr7:150705614-150706020	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr7:150704584-150707060	K562	blood:	n/a	n/a
21	CBX3	chr7:150705114-150706132	K562	blood:	n/a	n/a
22	CBX3	chr7:150707102-150708607	K562	blood:	n/a	n/a
23	CBX3	chr7:150700524-150701076	K562	blood:	n/a	n/a
24	CCNT2	chr7:150707232-150707920	K562	blood:	n/a	n/a
25	CCNT2	chr7:150706484-150706915	K562	blood:	n/a	n/a
26	CCNT2	chr7:150704517-150704594	K562	blood:	n/a	n/a
27	CCNT2	chr7:150705157-150706237	K562	blood:	n/a	n/a
28	CEBPB	chr7:150705104-150706135	K562	blood:	n/a	chr7:150705403-150705411
29	CEBPB	chr7:150705042-150706070	K562	blood:	n/a	chr7:150705403-150705411
30	CEBPD	chr7:150705057-150706081	K562	blood:	n/a	n/a
31	CEBPD	chr7:150705686-150706009	HepG2	liver:	n/a	n/a
32	CEBPD	chr7:150704723-150706889	K562	blood:	n/a	n/a
33	CHD2	chr7:150705857-150706057	HepG2	liver:	n/a	n/a
34	CHD2	chr7:150707013-150707140	K562	blood:	n/a	n/a
35	CHD2	chr7:150705249-150706411	K562	blood:	n/a	chr7:150706263-150706273
36	CHD2	chr7:150706272-150706275	HepG2	liver:	n/a	n/a
37	CHD2	chr7:150707430-150707989	K562	blood:	n/a	n/a
38	CHD2	chr7:150707587-150707851	HepG2	liver:	n/a	n/a
39	CHD2	chr7:150707494-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr7:150705671-150706146	GM12878	blood:	n/a	n/a
41	CHD2	chr7:150705619-150706076	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr7:150706720-150706870	HRE	kidney:	n/a	n/a
43	CTCF	chr7:150706540-150706690	HMF	breast:	n/a	n/a
44	CTCF	chr7:150706320-150706470	GM12867	blood:	n/a	n/a
45	CTCF	chr7:150705880-150706030	GM12872	blood:	n/a	n/a
46	CTCF	chr7:150705920-150706070	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr7:150706380-150706530	HRE	kidney:	n/a	n/a
48	CTCF	chr7:150705603-150707136	K562	blood:	n/a	n/a
49	CTCF	chr7:150706480-150706630	AG04449	skin:	n/a	n/a
50	CTCF	chr7:150706403-150706966	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150706268-150706318	HCM	heart:	n/a
2	chr7:150706268-150706318	HCT-116	colon:	n/a
3	chr7:150706268-150706318	HCM	heart:	n/a
4	chr7:150706268-150706318	HCT-116	colon:	n/a
5	chr7:150703765-150703815	BJ	skin:	n/a
6	chr7:150705760-150705810	PANC-1	pancreas:	n/a
7	chr7:150705896-150705946	BJ	skin:	n/a
8	chr7:150703765-150703815	K562	blood:	n/a
9	chr7:150706268-150706318	A549	lung:	n/a
10	chr7:150705872-150705922	MCF10A-Er-Src	breast:	n/a
11	chr7:150706268-150706318	AG04450	lung:	fetal
12	chr7:150707830-150707880	Hela-S3	cervix:	n/a
13	chr7:150706128-150706178	AG04450	lung:	fetal
14	chr7:150706268-150706318	AG04449	skin:	fetal
15	chr7:150705896-150705946	HMEC	breast:	n/a
16	chr7:150705896-150705946	IMR90	lung:	fetal
17	chr7:150703765-150703815	HCT-116	colon:	n/a
18	chr7:150705872-150705922	HIPEpiC	eye:	n/a
19	chr7:150707313-150707363	HRCEpiC	kidney:	n/a
20	chr7:150705000-150705050	AG10803	skin:	n/a
21	chr7:150705872-150705922	SK-N-MC	brain:	n/a
22	chr7:150705760-150705810	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:150706268-150706318	HMEC	breast:	n/a
24	chr7:150706355-150706405	AG10803	skin:	n/a
25	chr7:150706268-150706318	HRPEpiC	eye:	n/a
26	chr7:150707830-150707880	SKMC	muscle:	n/a
27	chr7:150707830-150707880	HRPEpiC	eye:	n/a
28	chr7:150705000-150705050	HL-60	blood:	n/a
29	chr7:150707830-150707880	HAEpiC	amniotic membrane:	n/a
30	chr7:150702471-150702521	ECC-1	luminal epithelium:	n/a
31	chr7:150703765-150703815	HRE	kidney:	n/a
32	chr7:150706355-150706405	AG04450	lung:	fetal
33	chr7:150705896-150705946	Jurkat	blood:	n/a
34	chr7:150706128-150706178	RPTEC	kidney:	n/a
35	chr7:150707830-150707880	BE2_C	brain:	n/a
36	chr7:150705000-150705050	AG09319	gingival:	n/a
37	chr7:150707313-150707363	AG04449	skin:	fetal
38	chr7:150706268-150706318	GM06990	blood:	n/a
39	chr7:150707830-150707880	NHBE	bronchial:	n/a
40	chr7:150705760-150705810	HUVEC	blood vessel:	n/a
41	chr7:150705760-150705810	GM12878	blood:	n/a
42	chr7:150707313-150707363	PrEC	prostate:	n/a
43	chr7:150706355-150706405	HMEC	breast:	n/a
44	chr7:150703765-150703815	HL-60	blood:	n/a
45	chr7:150706321-150706371	HCF	heart:	n/a
46	chr7:150702471-150702521	HRE	kidney:	n/a
47	chr7:150705760-150705810	AG09319	gingival:	n/a
48	chr7:150702471-150702521	PANC-1	pancreas:	n/a
49	chr7:150703765-150703815	SKMC	muscle:	n/a
50	chr7:150705896-150705946	GM12891	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150706188..150708123-chr7:150710621..150712135,2	MCF-7	breast:
2	chr7:150697364..150699402-chr7:150699417..150701595,2	MCF-7	breast:
3	chr7:150705619..150708029-chr7:150714028..150715967,2	MCF-7	breast:
4	chr7:150703619..150706319-chr7:150708116..150709799,2	MCF-7	breast:
5	chr7:150674597..150677558-chr7:150699359..150702536,4	MCF-7	breast:
6	chr7:150702588..150705432-chr7:150714534..150717607,5	MCF-7	breast:
7	chr7:150705881..150707323-chr7:150714964..150716387,6	K562	blood:
8	chr7:150705481..150706887-chr7:150725454..150726471,3	K562	blood:
9	chr1:201951630..201952197-chr7:150703679..150704350,2	HCT-116	colon:
10	chr7:150699504..150701651-chr7:150755109..150756845,2	MCF-7	breast:
11	chr7:150570280..150573172-chr7:150702825..150704695,2	K562	blood:

No data

Variant related genes	Relation type
NOS3	TF binding region
NOS3	CpG island
ENSG00000181652	chromatin interactions
ENSG00000055118	chromatin interactions
ENSG00000164889	chromatin interactions
ENSG00000164867	chromatin interactions
ENSG00000176393	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000197150	chromatin interactions

Extended variants
information (count: 340 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575926196	chr7:150701060-150701061	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs530064692	chr7:150701068-150701069	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs546681441	chr7:150701092-150701093	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs544135117	chr7:150701125-150701126	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs566575203	chr7:150701136-150701137	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs2853794	chr7:150701155-150701156	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs370223468	chr7:150701192-150701193	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs7776461	chr7:150701241-150701242	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs570567935	chr7:150701254-150701255	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs3918178	chr7:150701279-150701280	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs3918179	chr7:150701298-150701299	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs554816364	chr7:150701330-150701331	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs574645522	chr7:150701370-150701371	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs534140998	chr7:150701451-150701452	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs553477874	chr7:150701628-150701629	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576946949	chr7:150701648-150701649	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs545891283	chr7:150701678-150701679	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542315150	chr7:150701685-150701686	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186849056	chr7:150701686-150701687	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs143531681	chr7:150701724-150701725	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544488322	chr7:150701730-150701731	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs2566510	chr7:150701737-150701738	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs3918180	chr7:150701755-150701756	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs3918181	chr7:150701783-150701784	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs547313927	chr7:150701796-150701797	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60848465	chr7:150701836-150701837	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs532401138	chr7:150701843-150701844	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182553063	chr7:150701856-150701857	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs3918228	chr7:150701858-150701859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116566832	chr7:150701901-150701902	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115533949	chr7:150701904-150701905	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531201274	chr7:150701927-150701928	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571188311	chr7:150701931-150701932	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527556926	chr7:150701935-150701936	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs547586651	chr7:150701938-150701939	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368836761	chr7:150701944-150701945	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs147104368	chr7:150701948-150701949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574392846	chr7:150701952-150701953	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs187335619	chr7:150702007-150702008	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs370521303	chr7:150702039-150702040	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572268702	chr7:150702040-150702041	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374749514	chr7:150702043-150702044	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554135868	chr7:150702049-150702050	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs3918182	chr7:150702071-150702072	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539455059	chr7:150702094-150702095	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556253071	chr7:150702136-150702137	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576059530	chr7:150702137-150702138	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541955719	chr7:150702147-150702148	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554498375	chr7:150702158-150702159	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs3918183	chr7:150702191-150702192	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150692200-150705000	Weak transcription	Ovary	ovary
2	chr7:150692400-150704200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:150692400-150704400	Weak transcription	Right Atrium	heart
4	chr7:150692600-150704000	Weak transcription	Left Ventricle	heart
5	chr7:150694400-150704400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:150694600-150705600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:150694800-150704800	Weak transcription	Fetal Lung	lung
8	chr7:150694800-150705200	Weak transcription	Fetal Intestine Small	intestine
9	chr7:150695000-150705400	Weak transcription	Fetal Intestine Large	intestine
10	chr7:150695600-150704600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:150697000-150704000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr7:150697600-150701400	Genic enhancers	Placenta	Placenta
13	chr7:150697600-150703800	Weak transcription	Primary T cells from cord blood	blood
14	chr7:150697800-150703600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr7:150697800-150704400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr7:150698200-150703800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr7:150698200-150704000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:150698200-150704000	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr7:150698200-150704200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:150698400-150703800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:150699000-150703600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr7:150699200-150704200	Weak transcription	Right Ventricle	heart
23	chr7:150699400-150702200	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr7:150699400-150703600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:150699800-150702400	Weak transcription	Spleen	Spleen
26	chr7:150699800-150703600	Weak transcription	Lung	lung
27	chr7:150699800-150706600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:150700000-150702200	Weak transcription	Adipose Nuclei	Adipose
29	chr7:150700200-150704000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr7:150700400-150704400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:150700600-150704200	Weak transcription	Stomach Smooth Muscle	stomach
32	chr7:150701000-150702200	Enhancers	HUVEC	blood vessel
33	chr7:150701000-150702400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr7:150701000-150702600	Enhancers	HepG2	liver
35	chr7:150701000-150704000	Weak transcription	Gastric	stomach
36	chr7:150701000-150704400	Weak transcription	K562	blood
37	chr7:150701000-150704800	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr7:150701000-150706800	Weak transcription	A549	lung
39	chr7:150701400-150703600	Strong transcription	Placenta	Placenta
40	chr7:150702200-150702400	Weak transcription	HUVEC	blood vessel
41	chr7:150702200-150702600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
42	chr7:150702200-150703000	Strong transcription	Adipose Nuclei	Adipose
43	chr7:150702200-150704600	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr7:150702400-150702600	Genic enhancers	Spleen	Spleen
45	chr7:150702400-150702800	Genic enhancers	HUVEC	blood vessel
46	chr7:150702400-150703400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr7:150702600-150703000	Flanking Active TSS	HepG2	liver
48	chr7:150702600-150703400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr7:150702600-150703600	Strong transcription	Spleen	Spleen
50	chr7:150702800-150703000	Strong transcription	HUVEC	blood vessel

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