Variant report

Variant	nsv888650
Chromosome Location	chr7:85138665-85267174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:85194316-85194431	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:85183644-85184017	HepG2	liver:	n/a	n/a
3	ATF1	chr7:85210707-85210842	K562	blood:	n/a	n/a
4	ATF1	chr7:85183590-85183761	K562	blood:	n/a	n/a
5	ATF1	chr7:85142385-85142483	K562	blood:	n/a	n/a
6	BACH1	chr7:85229703-85230012	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr7:85221189-85221679	A549	lung:	n/a	n/a
8	BHLHE40	chr7:85221305-85221476	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:85183697-85183834	K562	blood:	n/a	n/a
10	CCNT2	chr7:85231581-85231835	K562	blood:	n/a	n/a
11	CEBPB	chr7:85157958-85158361	IMR90	lung:	n/a	chr7:85158198-85158209
12	CEBPB	chr7:85224999-85225591	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:85184159-85184489	IMR90	lung:	n/a	chr7:85184415-85184426 chr7:85184308-85184321 chr7:85184309-85184320 chr7:85184415-85184428 chr7:85184415-85184426
14	CEBPB	chr7:85183561-85183918	MCF-7	breast:	n/a	n/a
15	CEBPB	chr7:85178686-85178918	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:85260085-85260722	A549	lung:	n/a	n/a
17	CEBPB	chr7:85183697-85183965	A549	lung:	n/a	n/a
18	CEBPB	chr7:85255501-85255560	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:85178659-85178969	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:85158030-85158279	A549	lung:	n/a	chr7:85158198-85158209
21	CEBPB	chr7:85144481-85144935	IMR90	lung:	n/a	chr7:85144775-85144786
22	CEBPB	chr7:85158610-85158946	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:85260258-85260678	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:85183580-85183936	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:85158542-85158990	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr7:85225271-85225515	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:85145989-85146340	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:85184148-85184492	HepG2	liver:	n/a	chr7:85184415-85184426 chr7:85184308-85184321 chr7:85184309-85184320 chr7:85184415-85184428 chr7:85184415-85184426
29	CEBPB	chr7:85183484-85184075	A549	lung:	n/a	n/a
30	CEBPB	chr7:85251491-85251687	A549	lung:	n/a	n/a
31	CEBPB	chr7:85266317-85266413	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:85149736-85149983	Hela-S3	cervix:	n/a	chr7:85149814-85149825 chr7:85149814-85149827
33	CEBPB	chr7:85138256-85138809	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:85229849-85230092	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:85260254-85260658	A549	lung:	n/a	n/a
36	CEBPB	chr7:85158711-85158903	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:85183602-85184478	A549	lung:	n/a	chr7:85184415-85184426 chr7:85184308-85184321 chr7:85184309-85184320 chr7:85184415-85184428 chr7:85184415-85184426
38	CEBPB	chr7:85178678-85178883	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:85266363-85266490	A549	lung:	n/a	n/a
40	CEBPB	chr7:85183575-85183946	MCF-7	breast:	n/a	n/a
41	CEBPB	chr7:85183600-85183934	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:85183580-85183944	HepG2	liver:	n/a	n/a
43	CTCF	chr7:85183325-85184143	SK-N-SH	brain:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785
44	CTCF	chr7:85183660-85183810	HepG2	liver:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785
45	CTCF	chr7:85183629-85183907	Lung_OC	lung:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785
46	CTCF	chr7:85183680-85183830	HEEpiC	esophagus:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785
47	CTCF	chr7:85183720-85183870	GM12865	blood:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785
48	CTCF	chr7:85183740-85183890	HBMEC	blood vessel:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785
49	CTCF	chr7:85183700-85183850	AG04450	lung:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785
50	CTCF	chr7:85183584-85183938	Medullo	brain:	n/a	chr7:85183772-85183785 chr7:85183770-85183788 chr7:85183765-85183786 chr7:85183771-85183787 chr7:85183777-85183785

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:85157964-85158014	HRCEpiC	kidney:	n/a
2	chr7:85157964-85158014	PrEC	prostate:	n/a
3	chr7:85151454-85151504	SK-N-MC	brain:	n/a
4	chr7:85151454-85151504	U87	brain:	n/a
5	chr7:85151454-85151504	BE2_C	brain:	n/a
6	chr7:85151454-85151504	HEEpiC	esophagus:	n/a
7	chr7:85151454-85151504	CMK	blood:	n/a
8	chr7:85151454-85151504	K562	blood:	n/a
9	chr7:85157964-85158014	H1-hESC	embryonic stem cell:	embryo
10	chr7:85151454-85151504	LNCaP	prostate:	n/a
11	chr7:85151454-85151504	HAEpiC	amniotic membrane:	n/a
12	chr7:85151454-85151504	SAEC	small airway:	n/a
13	chr7:85151454-85151504	Caco-2	colon:	n/a
14	chr7:85151454-85151504	T-47D	breast:	n/a
15	chr7:85151454-85151504	HCF	heart:	n/a
16	chr7:85151454-85151504	AG04449	skin:	fetal
17	chr7:85157964-85158014	ovcar-3	ovarian:	n/a
18	chr7:85151454-85151504	HCT-116	colon:	n/a
19	chr7:85157964-85158014	Caco-2	colon:	n/a
20	chr7:85157964-85158014	HEK293	kidney:	embryo
21	chr7:85157964-85158014	HUVEC	blood vessel:	n/a
22	chr7:85157964-85158014	Hela-S3	cervix:	n/a
23	chr7:85151454-85151504	MCF-7	breast:	n/a
24	chr7:85151454-85151504	HUVEC	blood vessel:	n/a
25	chr7:85157964-85158014	U87	brain:	n/a
26	chr7:85157964-85158014	HepG2	liver:	n/a
27	chr7:85157964-85158014	HL-60	blood:	n/a
28	chr7:85151454-85151504	HepG2	liver:	n/a
29	chr7:85151454-85151504	AG09319	gingival:	n/a
30	chr7:85157964-85158014	BJ	skin:	n/a
31	chr7:85151454-85151504	NB4	blood:	n/a
32	chr7:85151454-85151504	HRCEpiC	kidney:	n/a
33	chr7:85157964-85158014	AoSMC	blood vessel:	n/a
34	chr7:85157964-85158014	NHDF-neo	bronchial:	n/a
35	chr7:85157964-85158014	PANC-1	pancreas:	n/a
36	chr7:85157964-85158014	HMEC	breast:	n/a
37	chr7:85157964-85158014	GM12892	blood:	n/a
38	chr7:85151454-85151504	AG09309	skin:	n/a
39	chr7:85151454-85151504	HMEC	breast:	n/a
40	chr7:85157964-85158014	GM19239	blood:	n/a
41	chr7:85157964-85158014	HRE	kidney:	n/a
42	chr7:85151454-85151504	IMR90	lung:	fetal
43	chr7:85157964-85158014	SK-N-MC	brain:	n/a
44	chr7:85157964-85158014	NHBE	bronchial:	n/a
45	chr7:85151454-85151504	NHDF-neo	bronchial:	n/a
46	chr7:85151454-85151504	HIPEpiC	eye:	n/a
47	chr7:85157964-85158014	BE2_C	brain:	n/a
48	chr7:85151454-85151504	A549	lung:	n/a
49	chr7:85151454-85151504	HL-60	blood:	n/a
50	chr7:85157964-85158014	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:85224212..85226454-chr7:85229348..85230972,2	MCF-7	breast:
2	chr7:85144834..85146430-chr7:85147566..85149706,2	K562	blood:
3	chr7:84659480..84660360-chr7:85183314..85184162,2	MCF-7	breast:
4	chr7:85183273..85184394-chr7:85379037..85380205,4	MCF-7	breast:
5	chr7:85253799..85255323-chr7:85392933..85394931,2	K562	blood:
6	chr7:85144834..85146430-chr7:85147566..85149706,2	K562	blood:
7	chr7:85153959..85156643-chr7:85186340..85188558,2	K562	blood:
8	chr12:7024083..7024583-chr7:85192420..85193063,2	MCF-7	breast:
9	chr7:85134714..85136666-chr7:85145066..85147658,2	K562	blood:
10	chr7:85153959..85156643-chr7:85186340..85188558,2	K562	blood:
11	chr7:85224212..85226454-chr7:85229348..85230972,2	MCF-7	breast:
12	chr7:84670622..84671190-chr7:85183449..85184130,2	MCF-7	breast:
13	chr7:84671065..84671572-chr7:85183760..85184324,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA3D-4	chr7:85265329-85265660	NONHSAT121800

Variant related genes	Relation type
ENSG00000227785	TF binding region
ENSG00000227785	CpG island
ENSG00000153993	chromatin interactions
ENSG00000111674	chromatin interactions

Extended variants
information (count: 3036 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3036 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2498539	chr7:85138665-85138666	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577051481	chr7:85138690-85138691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544119874	chr7:85138696-85138697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188765735	chr7:85138712-85138713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2498538	chr7:85138729-85138730	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs201706154	chr7:85138738-85138739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74349365	chr7:85138758-85138759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112208342	chr7:85138760-85138761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73703668	chr7:85138798-85138799	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs377545678	chr7:85138842-85138843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35318163	chr7:85138895-85138896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552526134	chr7:85138898-85138899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571095797	chr7:85138906-85138907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550692629	chr7:85138914-85138915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142180282	chr7:85138920-85138921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2247661	chr7:85138935-85138936	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs150165226	chr7:85139076-85139077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535617906	chr7:85139093-85139094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114695238	chr7:85139109-85139110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117873829	chr7:85139125-85139126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181239047	chr7:85139127-85139128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558516615	chr7:85139150-85139151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12112405	chr7:85139197-85139198	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs544499205	chr7:85139207-85139208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562601957	chr7:85139216-85139217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536475949	chr7:85139221-85139222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531809698	chr7:85139248-85139249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186516603	chr7:85139260-85139261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542019833	chr7:85139263-85139264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2372789	chr7:85139317-85139318	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs202075433	chr7:85139335-85139336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527774091	chr7:85139336-85139337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552332941	chr7:85139342-85139343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533886653	chr7:85139366-85139367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73391556	chr7:85139400-85139401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558525321	chr7:85139464-85139465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs13238520	chr7:85139469-85139470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531565055	chr7:85139506-85139507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550464528	chr7:85139539-85139540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568385391	chr7:85139579-85139580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189837857	chr7:85139613-85139614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6951975	chr7:85139675-85139676	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566272081	chr7:85139719-85139720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2463683	chr7:85139756-85139757	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs537936704	chr7:85139806-85139807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs180987569	chr7:85139813-85139814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570713983	chr7:85139867-85139868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112418411	chr7:85139903-85139904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556099967	chr7:85139922-85139923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs57360737	chr7:85139954-85139955	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:85137600-85139200	Enhancers	NHLF	lung
2	chr7:85137800-85139200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:85137800-85139200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:85138000-85139000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:85138000-85139000	Enhancers	NH-A	brain
6	chr7:85138000-85139000	Enhancers	NHDF-Ad	bronchial
7	chr7:85138000-85139200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:85138000-85139800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:85138200-85139000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:85138200-85139200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:85139000-85139400	Enhancers	Placenta Amnion	Placenta Amnion
12	chr7:85139000-85139800	Weak transcription	NHDF-Ad	bronchial
13	chr7:85139000-85146200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:85139200-85144000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:85139200-85144000	Weak transcription	NHLF	lung
16	chr7:85139200-85144400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:85139800-85140000	Enhancers	NHDF-Ad	bronchial
18	chr7:85139800-85145800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:85143800-85144600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:85144000-85144600	Enhancers	NHLF	lung
21	chr7:85144000-85144800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:85144400-85144800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:85144400-85144800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:85144600-85145400	Weak transcription	NHLF	lung
25	chr7:85144800-85145800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:85145800-85146000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:85145800-85146400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:85146200-85146400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:85146400-85150800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:85146600-85150600	Weak transcription	Fetal Kidney	kidney
31	chr7:85149200-85150600	Enhancers	Fetal Lung	lung
32	chr7:85149600-85150000	Enhancers	Fetal Stomach	stomach
33	chr7:85150000-85150400	Weak transcription	Fetal Stomach	stomach
34	chr7:85150400-85151000	Enhancers	Colon Smooth Muscle	Colon
35	chr7:85150400-85151000	Enhancers	Fetal Stomach	stomach
36	chr7:85150400-85151000	Enhancers	NHLF	lung
37	chr7:85150600-85150800	Flanking Active TSS	Fetal Lung	lung
38	chr7:85150600-85151000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr7:85150600-85151000	Enhancers	Fetal Heart	heart
40	chr7:85150800-85151000	Enhancers	Fetal Kidney	kidney
41	chr7:85150800-85151000	Enhancers	Fetal Lung	lung
42	chr7:85150800-85151000	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr7:85150800-85151200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:85150800-85151200	Enhancers	Small Intestine	intestine
45	chr7:85151000-85151200	Flanking Active TSS	Fetal Lung	lung
46	chr7:85151000-85154800	Weak transcription	NHLF	lung
47	chr7:85151200-85152600	Enhancers	Fetal Lung	lung
48	chr7:85151200-85158000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:85152600-85155000	Weak transcription	Fetal Lung	lung
50	chr7:85153400-85153800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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