Variant report

Variant	nsv1034546
Chromosome Location	chr7:136832263-136858804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:269)
CpG islands
(count:488)
Chromatin interactive
region (count:11)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:136853987-136854164	HepG2	liver:	n/a	n/a
2	ATF2	chr7:136853857-136854307	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:136853848-136854381	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:136853886-136854162	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:136856791-136856855	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:136856746-136856949	IMR90	lung:	n/a	chr7:136856865-136856876
7	CEBPB	chr7:136835316-136835641	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:136851292-136851308	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:136856710-136857042	HepG2	liver:	n/a	chr7:136856865-136856876
10	CEBPB	chr7:136851161-136851454	IMR90	lung:	n/a	chr7:136851307-136851316
11	CEBPB	chr7:136856735-136856935	A549	lung:	n/a	chr7:136856865-136856876
12	CEBPB	chr7:136853989-136854249	H1-hESC	embryonic stem cell:	n/a	chr7:136854153-136854165
13	CEBPB	chr7:136851211-136851370	K562	blood:	n/a	chr7:136851307-136851316
14	CHD2	chr7:136853979-136854259	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr7:136854040-136854190	HAc	cerebellar:	n/a	chr7:136854107-136854128
16	CTCF	chr7:136854040-136854190	GM12864	blood:	n/a	chr7:136854107-136854128
17	CTCF	chr7:136854060-136854210	RPTEC	kidney:	n/a	chr7:136854107-136854128
18	CTCF	chr7:136854000-136854150	HRPEpiC	eye:	n/a	chr7:136854107-136854128
19	CTCF	chr7:136854000-136854150	GM12878	blood:	n/a	chr7:136854107-136854128
20	CTCF	chr7:136854020-136854170	BE2_C	brain:	n/a	chr7:136854107-136854128
21	CTCF	chr7:136854080-136854230	GM12864	blood:	n/a	chr7:136854107-136854128
22	CTCF	chr7:136854020-136854170	A549	lung:	n/a	chr7:136854107-136854128
23	CTCF	chr7:136854040-136854190	NHDF-neo	bronchial:	n/a	chr7:136854107-136854128
24	CTCF	chr7:136853988-136854227	HUVEC	blood vessel:	n/a	chr7:136854107-136854128
25	CTCF	chr7:136853957-136854257	MCF-7	breast:	n/a	chr7:136854107-136854128
26	CTCF	chr7:136854015-136854206	GM12891	blood:	n/a	chr7:136854107-136854128
27	CTCF	chr7:136854020-136854170	HEK293	kidney:	n/a	chr7:136854107-136854128
28	CTCF	chr7:136844040-136844190	AG09319	gingival:	n/a	n/a
29	CTCF	chr7:136854020-136854170	MCF-7	breast:	n/a	chr7:136854107-136854128
30	CTCF	chr7:136853978-136854239	LNCaP	prostate:	n/a	chr7:136854107-136854128
31	CTCF	chr7:136854020-136854170	AG09309	skin:	n/a	chr7:136854107-136854128
32	CTCF	chr7:136854020-136854170	AG09319	gingival:	n/a	chr7:136854107-136854128
33	CTCF	chr7:136853977-136854299	K562	blood:	n/a	chr7:136854107-136854128
34	CTCF	chr7:136853977-136854302	A549	lung:	n/a	chr7:136854107-136854128
35	CTCF	chr7:136854060-136854210	GM06990	blood:	n/a	chr7:136854107-136854128
36	CTCF	chr7:136853951-136854299	SK-N-SH_RA	brain:	n/a	chr7:136854107-136854128
37	CTCF	chr7:136854040-136854190	Caco-2	colon:	n/a	chr7:136854107-136854128
38	CTCF	chr7:136854040-136854190	HUVEC	blood vessel:	n/a	chr7:136854107-136854128
39	CTCF	chr7:136854020-136854170	GM12873	blood:	n/a	chr7:136854107-136854128
40	CTCF	chr7:136853966-136854284	ProgFib	skin:	n/a	chr7:136854107-136854128
41	CTCF	chr7:136854040-136854190	HBMEC	blood vessel:	n/a	chr7:136854107-136854128
42	CTCF	chr7:136854020-136854170	NHEK	skin:	n/a	chr7:136854107-136854128
43	CTCF	chr7:136854060-136854210	WI-38	lung:	n/a	chr7:136854107-136854128
44	CTCF	chr7:136854040-136854190	HCFaa	heart:	n/a	chr7:136854107-136854128
45	CTCF	chr7:136853987-136854221	Pancreas_OC	pancreas:	n/a	chr7:136854107-136854128
46	CTCF	chr7:136853987-136854233	A549	lung:	n/a	chr7:136854107-136854128
47	CTCF	chr7:136854040-136854190	K562	blood:	n/a	chr7:136854107-136854128
48	CTCF	chr7:136853980-136854130	HFF-Myc	foreskin:	n/a	chr7:136854107-136854128
49	CTCF	chr7:136853760-136853910	K562	blood:	n/a	n/a
50	CTCF	chr7:136854023-136854218	Spleen_OC	spleen:	n/a	chr7:136854107-136854128

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:136849317-136849367	CMK	blood:	n/a
2	chr7:136850736-136850786	Hela-S3	cervix:	n/a
3	chr7:136849187-136849237	BE2_C	brain:	n/a
4	chr7:136849262-136849312	HRE	kidney:	n/a
5	chr7:136832262-136832312	Caco-2	colon:	n/a
6	chr7:136849143-136849193	AG04450	lung:	fetal
7	chr7:136832262-136832312	HCF	heart:	n/a
8	chr7:136850736-136850786	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:136849317-136849367	AG04450	lung:	fetal
10	chr7:136849143-136849193	Caco-2	colon:	n/a
11	chr7:136849262-136849312	HRCEpiC	kidney:	n/a
12	chr7:136849143-136849193	HRCEpiC	kidney:	n/a
13	chr7:136849262-136849312	ovcar-3	ovarian:	n/a
14	chr7:136849018-136849068	AG09309	skin:	n/a
15	chr7:136850736-136850786	NT2-D1	testis:	n/a
16	chr7:136849143-136849193	NT2-D1	testis:	n/a
17	chr7:136849317-136849367	HRE	kidney:	n/a
18	chr7:136849143-136849193	AG10803	skin:	n/a
19	chr7:136850736-136850786	GM12891	blood:	n/a
20	chr7:136849187-136849237	H1-hESC	embryonic stem cell:	embryo
21	chr7:136849317-136849367	HCF	heart:	n/a
22	chr7:136849018-136849068	Hela-S3	cervix:	n/a
23	chr7:136849187-136849237	Hela-S3	cervix:	n/a
24	chr7:136849187-136849237	AG09309	skin:	n/a
25	chr7:136849143-136849193	AoSMC	blood vessel:	n/a
26	chr7:136849018-136849068	SAEC	small airway:	n/a
27	chr7:136845265-136845315	H1-hESC	embryonic stem cell:	embryo
28	chr7:136849317-136849367	HIPEpiC	eye:	n/a
29	chr7:136850736-136850786	HCM	heart:	n/a
30	chr7:136849262-136849312	PrEC	prostate:	n/a
31	chr7:136845265-136845315	HCF	heart:	n/a
32	chr7:136832262-136832312	GM19239	blood:	n/a
33	chr7:136849262-136849312	CMK	blood:	n/a
34	chr7:136849262-136849312	BJ	skin:	n/a
35	chr7:136849143-136849193	MCF-7	breast:	n/a
36	chr7:136849187-136849237	A549	lung:	n/a
37	chr7:136849187-136849237	K562	blood:	n/a
38	chr7:136849317-136849367	AG04449	skin:	fetal
39	chr7:136849317-136849367	MCF-7	breast:	n/a
40	chr7:136849317-136849367	Jurkat	blood:	n/a
41	chr7:136849018-136849068	ovcar-3	ovarian:	n/a
42	chr7:136845265-136845315	Caco-2	colon:	n/a
43	chr7:136849143-136849193	BJ	skin:	n/a
44	chr7:136832262-136832312	GM12892	blood:	n/a
45	chr7:136832262-136832312	HCT-116	colon:	n/a
46	chr7:136849262-136849312	HMEC	breast:	n/a
47	chr7:136845265-136845315	SK-N-SH_RA	brain:	n/a
48	chr7:136849187-136849237	AG09319	gingival:	n/a
49	chr7:136849317-136849367	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:136849187-136849237	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:136853692..136854573-chr7:137276894..137277671,4	MCF-7	breast:
2	chr7:136854007..136854801-chr7:137137517..137138269,2	MCF-7	breast:
3	chr7:136845496..136847194-chr7:136910849..136912754,2	MCF-7	breast:
4	chr2:196521592..196522296-chr7:136849044..136849880,2	HCT-116	colon:
5	chr4:150815194..150816071-chr7:136849876..136850472,2	MCF-7	breast:
6	chr7:136853367..136854657-chr7:137138615..137139665,11	MCF-7	breast:
7	chr7:136853636..136854568-chr7:137022322..137023760,5	MCF-7	breast:
8	chr7:136853684..136854424-chr7:137022605..137023178,2	MCF-7	breast:
9	chr7:136853835..136854630-chr7:137138677..137139572,6	MCF-7	breast:
10	chr7:136858672..136861163-chr7:136864097..136866322,2	K562	blood:
11	chr7:136853682..136854530-chr7:137276883..137277639,5	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTN-2	chr7:136848868-136849017	ENSG00000234352.5
2	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
3	lnc-PTN-2	chr7:136848868-136849020	ENSG00000234352.5
4	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
5	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352.2
6	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352
7	lnc-PTN-2	chr7:136848868-136849017	NONHSAT123574
8	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5

No data

Variant related genes	Relation type
ENSG00000224469	TF binding region
ENSG00000234352	TF binding region
ENSG00000224469	CpG island
ENSG00000234352	CpG island
ENSG00000157680	chromatin interactions
ENSG00000196950	chromatin interactions
SLC35B4	miRNA target sites

Extended variants
information (count: 713 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs832969	chr7:136832263-136832264	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373015277	chr7:136832264-136832265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562908068	chr7:136832275-136832276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140665942	chr7:136832286-136832287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs832968	chr7:136832300-136832301	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs561967025	chr7:136832326-136832327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73727844	chr7:136832334-136832335	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527924906	chr7:136832335-136832336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117616459	chr7:136832342-136832343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567297533	chr7:136832356-136832357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547501858	chr7:136832402-136832403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536236685	chr7:136832431-136832432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372605245	chr7:136832438-136832439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117820396	chr7:136832480-136832481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144372807	chr7:136832482-136832483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540999255	chr7:136832488-136832489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538518182	chr7:136832568-136832569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151067396	chr7:136832571-136832572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192773182	chr7:136832590-136832591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534552902	chr7:136832591-136832592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs832967	chr7:136832667-136832668	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs184747156	chr7:136832701-136832702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543108297	chr7:136832711-136832712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562709592	chr7:136832737-136832738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576518234	chr7:136832739-136832740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549330718	chr7:136832766-136832767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545703434	chr7:136832773-136832774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189263240	chr7:136832786-136832787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565608020	chr7:136832792-136832793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527887834	chr7:136832821-136832822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547716954	chr7:136832903-136832904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562216242	chr7:136832909-136832910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180690709	chr7:136832958-136832959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185272187	chr7:136832968-136832969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569515821	chr7:136832976-136832977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538275495	chr7:136833045-136833046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552049557	chr7:136833068-136833069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565676694	chr7:136833097-136833098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534611409	chr7:136833108-136833109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs832966	chr7:136833126-136833127	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs141009434	chr7:136833164-136833165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536312685	chr7:136833178-136833179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189634171	chr7:136833202-136833203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181854599	chr7:136833250-136833251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186227385	chr7:136833302-136833303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562289614	chr7:136833324-136833325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191681413	chr7:136833342-136833343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565570568	chr7:136833370-136833371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572738426	chr7:136833374-136833375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74529490	chr7:136833376-136833377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136830200-136834000	Enhancers	Colon Smooth Muscle	Colon
2	chr7:136830200-136834400	Enhancers	Fetal Heart	heart
3	chr7:136830400-136832400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:136830400-136832400	Enhancers	HSMM	muscle
5	chr7:136830600-136832400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:136830600-136833800	Enhancers	Fetal Stomach	stomach
7	chr7:136830800-136833000	Enhancers	HSMMtube	muscle
8	chr7:136830800-136834000	Enhancers	Placenta Amnion	Placenta Amnion
9	chr7:136831000-136833000	Enhancers	Rectal Smooth Muscle	rectum
10	chr7:136831400-136833200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr7:136831600-136832600	Enhancers	NHLF	lung
12	chr7:136831800-136832400	Enhancers	HMEC	breast
13	chr7:136831800-136833000	Enhancers	NH-A	brain
14	chr7:136832000-136832400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:136832000-136832400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:136832000-136832800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:136832000-136832800	Enhancers	NHDF-Ad	bronchial
18	chr7:136832000-136832800	Enhancers	Osteobl	bone
19	chr7:136832000-136833800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:136832200-136832800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr7:136832200-136833200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:136832200-136833200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:136832200-136835600	Weak transcription	Fetal Kidney	kidney
24	chr7:136832400-136835800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:136832600-136833000	Weak transcription	NHLF	lung
26	chr7:136832800-136833000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:136832800-136835600	Weak transcription	Osteobl	bone
28	chr7:136833000-136833200	Enhancers	NHLF	lung
29	chr7:136833000-136833600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr7:136833000-136835600	Weak transcription	NH-A	brain
31	chr7:136833000-136838800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:136833200-136835200	Weak transcription	NHLF	lung
33	chr7:136833600-136833800	Enhancers	Rectal Smooth Muscle	rectum
34	chr7:136833800-136834800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr7:136833800-136835000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:136833800-136835200	Weak transcription	Fetal Stomach	stomach
37	chr7:136834000-136835200	Weak transcription	Colon Smooth Muscle	Colon
38	chr7:136834000-136835400	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr7:136834400-136834800	Weak transcription	Fetal Heart	heart
40	chr7:136834800-136835200	Enhancers	Fetal Heart	heart
41	chr7:136834800-136837200	Enhancers	Rectal Smooth Muscle	rectum
42	chr7:136835000-136836200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:136835200-136836400	Flanking Active TSS	Fetal Heart	heart
44	chr7:136835200-136836600	Enhancers	NHLF	lung
45	chr7:136835200-136836800	Enhancers	Fetal Stomach	stomach
46	chr7:136835200-136837200	Enhancers	Colon Smooth Muscle	Colon
47	chr7:136835400-136836800	Enhancers	Placenta Amnion	Placenta Amnion
48	chr7:136835600-136836400	Enhancers	Fetal Brain Male	brain
49	chr7:136835600-136836400	Enhancers	NH-A	brain
50	chr7:136835600-136836600	Enhancers	Osteobl	bone

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