Variant report

Variant	nsv1016669
Chromosome Location	chr7:127927963-127948122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:122)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:122 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:127939408-127939596	K562	blood:	n/a	n/a
2	BHLHE40	chr7:127938259-127938392	HepG2	liver:	n/a	n/a
3	CBX3	chr7:127931568-127932076	K562	blood:	n/a	n/a
4	CBX3	chr7:127931732-127932059	K562	blood:	n/a	n/a
5	CEBPB	chr7:127928259-127928550	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:127930433-127930580	HepG2	liver:	n/a	chr7:127930525-127930536
7	CEBPB	chr7:127930523-127930538	IMR90	lung:	n/a	chr7:127930525-127930536
8	CEBPB	chr7:127930403-127930544	K562	blood:	n/a	chr7:127930525-127930536
9	CEBPB	chr7:127945691-127945856	A549	lung:	n/a	n/a
10	CHD2	chr7:127939860-127939937	H1-hESC	embryonic stem cell:	n/a	n/a
11	E2F4	chr7:127945326-127945481	MCF10A-Er-Src	breast:	n/a	n/a
12	EP300	chr7:127938103-127938425	HepG2	liver:	n/a	n/a
13	FOXA1	chr7:127938029-127938377	HepG2	liver:	n/a	n/a
14	FOXA1	chr7:127932323-127932684	HepG2	liver:	n/a	n/a
15	FOXA2	chr7:127932146-127932867	A549	lung:	n/a	n/a
16	FOXA2	chr7:127932430-127932839	A549	lung:	n/a	n/a
17	GATA3	chr7:127928376-127928448	SH-SY5Y	brain:	n/a	n/a
18	GTF2F1	chr7:127939373-127939502	H1-hESC	embryonic stem cell:	n/a	n/a
19	GTF2F1	chr7:127939886-127939928	H1-hESC	embryonic stem cell:	n/a	n/a
20	HNF4A	chr7:127938172-127938410	HepG2	liver:	n/a	chr7:127938273-127938288 chr7:127938307-127938322
21	HNF4A	chr7:127938092-127938414	HepG2	liver:	n/a	chr7:127938273-127938288 chr7:127938307-127938322
22	KAP1	chr7:127931723-127932060	K562	blood:	n/a	n/a
23	MAFK	chr7:127944287-127944437	HepG2	liver:	n/a	n/a
24	MAFK	chr7:127944221-127944473	HepG2	liver:	n/a	n/a
25	MAX	chr7:127939158-127939580	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAX	chr7:127939987-127940170	H1-hESC	embryonic stem cell:	n/a	n/a
27	MYC	chr7:127939340-127939760	H1-hESC	embryonic stem cell:	n/a	n/a
28	NRF1	chr7:127947599-127947625	K562	blood:	n/a	n/a
29	POLR2A	chr7:127940661-127940933	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr7:127941340-127941609	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr7:127944444-127944976	K562	blood:	n/a	n/a
32	POLR2A	chr7:127945623-127945929	PFSK-1	brain:	n/a	n/a
33	POLR2A	chr7:127941938-127942169	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:127941472-127941925	PANC-1	pancreas:	n/a	n/a
35	POLR2A	chr7:127942277-127942286	MCF-7	breast:	n/a	n/a
36	POLR2A	chr7:127943178-127943891	K562	blood:	n/a	n/a
37	POLR2A	chr7:127941387-127942242	U87	brain:	n/a	n/a
38	POLR2A	chr7:127939289-127939329	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr7:127943242-127943650	K562	blood:	n/a	n/a
40	POLR2A	chr7:127941480-127942063	A549	lung:	n/a	n/a
41	POLR2A	chr7:127942399-127942423	K562	blood:	n/a	n/a
42	POLR2A	chr7:127944302-127944708	SK-N-MC	brain:	n/a	n/a
43	POLR2A	chr7:127941573-127941575	HepG2	liver:	n/a	n/a
44	POLR2A	chr7:127945508-127946971	K562	blood:	n/a	n/a
45	POLR2A	chr7:127946991-127947537	K562	blood:	n/a	n/a
46	POLR2A	chr7:127942178-127942194	HepG2	liver:	n/a	n/a
47	POLR2A	chr7:127943243-127943507	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr7:127944512-127944639	GM12878	blood:	n/a	n/a
49	POLR2A	chr7:127930818-127930956	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr7:127945512-127946419	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127940559-127940609	HNPCEpiC	eye:	n/a
2	chr7:127940559-127940609	IMR90	lung:	fetal
3	chr7:127940559-127940609	GM19239	blood:	n/a
4	chr7:127940559-127940609	Jurkat	blood:	n/a
5	chr7:127940559-127940609	SK-N-MC	brain:	n/a
6	chr7:127940559-127940609	SK-N-SH_RA	brain:	n/a
7	chr7:127940559-127940609	CMK	blood:	n/a
8	chr7:127940559-127940609	PrEC	prostate:	n/a
9	chr7:127940559-127940609	PANC-1	pancreas:	n/a
10	chr7:127940559-127940609	GM12892	blood:	n/a
11	chr7:127940559-127940609	AG09319	gingival:	n/a
12	chr7:127940559-127940609	T-47D	breast:	n/a
13	chr7:127940559-127940609	NB4	blood:	n/a
14	chr7:127940559-127940609	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:127940559-127940609	HepG2	liver:	n/a
16	chr7:127940559-127940609	HIPEpiC	eye:	n/a
17	chr7:127940559-127940609	SKMC	muscle:	n/a
18	chr7:127940559-127940609	NH-A	brain:	n/a
19	chr7:127940559-127940609	Hela-S3	cervix:	n/a
20	chr7:127940559-127940609	K562	blood:	n/a
21	chr7:127940559-127940609	SK-N-SH	brain:	n/a
22	chr7:127940559-127940609	SAEC	small airway:	n/a
23	chr7:127940559-127940609	NT2-D1	testis:	n/a
24	chr7:127940559-127940609	NHDF-neo	bronchial:	n/a
25	chr7:127940559-127940609	Caco-2	colon:	n/a
26	chr7:127940559-127940609	BE2_C	brain:	n/a
27	chr7:127940559-127940609	HRPEpiC	eye:	n/a
28	chr7:127940559-127940609	HEK293	kidney:	embryo
29	chr7:127940559-127940609	Hepatocyte	liver:	n/a
30	chr7:127940559-127940609	MCF10A-Er-Src	breast:	n/a
31	chr7:127940559-127940609	HUVEC	blood vessel:	n/a
32	chr7:127940559-127940609	ECC-1	luminal epithelium:	n/a
33	chr7:127940559-127940609	HAEpiC	amniotic membrane:	n/a
34	chr7:127940559-127940609	AG04450	lung:	fetal
35	chr7:127940559-127940609	PFSK-1	brain:	n/a
36	chr7:127940559-127940609	NHBE	bronchial:	n/a
37	chr7:127940559-127940609	HMEC	breast:	n/a
38	chr7:127940559-127940609	A549	lung:	n/a
39	chr7:127940559-127940609	MCF-7	breast:	n/a
40	chr7:127940559-127940609	HCT-116	colon:	n/a
41	chr7:127940559-127940609	HEEpiC	esophagus:	n/a
42	chr7:127940559-127940609	LNCaP	prostate:	n/a
43	chr7:127940559-127940609	AG04449	skin:	fetal
44	chr7:127940559-127940609	ovcar-3	ovarian:	n/a
45	chr7:127940559-127940609	HRCEpiC	kidney:	n/a
46	chr7:127940559-127940609	HRE	kidney:	n/a
47	chr7:127940559-127940609	AoSMC	blood vessel:	n/a
48	chr7:127940559-127940609	GM12891	blood:	n/a
49	chr7:127940559-127940609	GM12878	blood:	n/a
50	chr7:127940559-127940609	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:127940082..127943532-chr7:127944561..127947795,4	K562	blood:
2	chr7:127946612..127948559-chr7:127954023..127956077,2	K562	blood:
3	chr7:127937053..127939817-chr7:127940949..127943521,2	K562	blood:
4	chr7:127940674..127942545-chr7:127948588..127950322,2	MCF-7	breast:
5	chr7:127941056..127943858-chr7:127948197..127950137,2	K562	blood:
6	chr7:127941056..127943858-chr7:127948197..127950566,3	K562	blood:
7	chr7:127937053..127939817-chr7:127940949..127943521,2	K562	blood:
8	chr7:127940019..127941640-chr7:127955342..127957765,2	K562	blood:
9	chr7:127940151..127942923-chr7:127964464..127966540,2	MCF-7	breast:
10	chr7:127938979..127940740-chr7:127949044..127951138,2	K562	blood:
11	chr7:127940010..127942133-chr7:127944769..127947134,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LEP-1	chr7:127946702-127947731	NONHSAT123181
2	lnc-RBM28-3	chr7:127944240-127946359	NONHSAT123179
3	lnc-RBM28-1	chr7:127930781-127931619	NONHSAT123176
4	lnc-RBM28-3	chr7:127937738-127947816	NONHSAT123178

No data

Variant related genes	Relation type
ENSG00000221429	TF binding region
ENSG00000242261	TF binding region
ENSG00000221429	CpG island
ENSG00000242261	CpG island
ENSG00000106344	chromatin interactions
ENSG00000242261	chromatin interactions

Extended variants
information (count: 717 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:717 , 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	rs17151967	chr7:127927963-127927964	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs578010274	chr7:127928020-127928021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545354115	chr7:127928044-127928045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560364140	chr7:127928086-127928087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371274503	chr7:127928100-127928101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34365144	chr7:127928115-127928116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531457856	chr7:127928171-127928172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185521075	chr7:127928199-127928200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs57060449	chr7:127928231-127928232	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs77106988	chr7:127928232-127928233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190005285	chr7:127928255-127928256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549389384	chr7:127928269-127928270	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs112413415	chr7:127928276-127928277	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs532652259	chr7:127928293-127928294	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs547711876	chr7:127928321-127928322	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs111822534	chr7:127928339-127928340	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs536861866	chr7:127928432-127928433	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs140629379	chr7:127928451-127928452	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs570153458	chr7:127928452-127928453	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs534037185	chr7:127928479-127928480	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs553685198	chr7:127928497-127928498	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537406864	chr7:127928553-127928554	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145429660	chr7:127928593-127928594	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577336843	chr7:127928619-127928620	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181701135	chr7:127928631-127928632	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117151952	chr7:127928658-127928659	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572107489	chr7:127928674-127928675	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76037807	chr7:127928694-127928695	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560796181	chr7:127928698-127928699	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576105069	chr7:127928699-127928700	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138040199	chr7:127928744-127928745	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76284662	chr7:127928775-127928776	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372847908	chr7:127928804-127928805	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186406875	chr7:127928814-127928815	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547675168	chr7:127928900-127928901	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559997211	chr7:127928916-127928917	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56091545	chr7:127928917-127928918	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs548779303	chr7:127928931-127928932	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570187695	chr7:127928953-127928954	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78046078	chr7:127928954-127928955	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552750090	chr7:127928962-127928963	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570849088	chr7:127928971-127928972	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535029012	chr7:127929000-127929001	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553738518	chr7:127929006-127929007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11772355	chr7:127929022-127929023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190184726	chr7:127929059-127929060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12534540	chr7:127929066-127929067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs141765698	chr7:127929085-127929086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150167441	chr7:127929117-127929118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558413934	chr7:127929121-127929122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Endometrioid adenocarcinoma	16974079	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
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127917000-127945600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:127917200-127943200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr7:127920200-127945200	Weak transcription	Right Ventricle	heart
4	chr7:127920600-127938800	Weak transcription	Right Atrium	heart
5	chr7:127920600-127941000	Weak transcription	Primary T cells from cord blood	blood
6	chr7:127920800-127931000	Weak transcription	Fetal Lung	lung
7	chr7:127921400-127939000	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr7:127921600-127928400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr7:127921800-127944400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr7:127922000-127940600	Weak transcription	Brain Anterior Caudate	brain
11	chr7:127922000-127942000	Weak transcription	Brain Angular Gyrus	brain
12	chr7:127922000-127944400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:127922200-127930800	Weak transcription	Brain Germinal Matrix	brain
14	chr7:127922200-127932600	Weak transcription	Fetal Intestine Small	intestine
15	chr7:127922200-127942000	Weak transcription	Left Ventricle	heart
16	chr7:127922200-127942200	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr7:127922200-127943000	Weak transcription	Dnd41	blood
18	chr7:127922200-127943200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr7:127922400-127932000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:127922400-127942000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:127923200-127929200	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr7:127923800-127928400	Weak transcription	HSMMtube	muscle
23	chr7:127923800-127943200	Weak transcription	Pancreas	Pancrea
24	chr7:127924000-127940000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr7:127924200-127943800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr7:127924400-127929200	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:127924400-127942200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:127924400-127942200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr7:127924600-127939000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:127924600-127940600	Weak transcription	A549	lung
31	chr7:127924600-127950000	Weak transcription	Psoas Muscle	Psoas
32	chr7:127926200-127940200	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr7:127926400-127930600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:127926400-127943200	Weak transcription	HSMM	muscle
35	chr7:127926600-127930400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:127926600-127931600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr7:127926600-127940600	Weak transcription	Liver	Liver
38	chr7:127926600-127941400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr7:127926800-127940400	Weak transcription	Stomach Smooth Muscle	stomach
40	chr7:127926800-127941400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr7:127927000-127931400	Weak transcription	Fetal Stomach	stomach
42	chr7:127927000-127932600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:127927000-127940400	Weak transcription	Aorta	Aorta
44	chr7:127927000-127940800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:127927000-127943200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:127927000-127944400	Weak transcription	Ovary	ovary
47	chr7:127928400-127928800	Enhancers	Rectal Smooth Muscle	rectum
48	chr7:127928400-127929000	Strong transcription	HSMMtube	muscle
49	chr7:127928600-127929000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:127928800-127944400	Weak transcription	Rectal Smooth Muscle	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links