Variant report

Variant	nsv981456
Chromosome Location	chr7:39431071-39454006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:492)
Chromatin interactive
region (count:7)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:39431848-39432018	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:39453441-39454296	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:39431880-39432090	GM12878	blood:	n/a	n/a
4	BHLHE40	chr7:39446015-39446266	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:39453754-39454208	GM12878	blood:	n/a	chr7:39454190-39454206
6	CCNT2	chr7:39453478-39453717	K562	blood:	n/a	n/a
7	CEBPB	chr7:39450244-39450515	MCF-7	breast:	n/a	chr7:39450347-39450358
8	CEBPB	chr7:39446117-39446375	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:39450225-39450478	Hela-S3	cervix:	n/a	chr7:39450347-39450358
10	CEBPB	chr7:39450262-39450475	IMR90	lung:	n/a	chr7:39450347-39450358
11	CEBPB	chr7:39450229-39450493	HepG2	liver:	n/a	chr7:39450347-39450358
12	CEBPB	chr7:39450229-39450465	A549	lung:	n/a	chr7:39450347-39450358
13	CEBPB	chr7:39450258-39450456	K562	blood:	n/a	chr7:39450347-39450358
14	CHD2	chr7:39453590-39454183	GM12878	blood:	n/a	n/a
15	CHD2	chr7:39453924-39454113	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr7:39453993-39454307	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr7:39454006-39454287	A549	lung:	n/a	n/a
18	CTCF	chr7:39453963-39454288	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr7:39454000-39454150	HEK293	kidney:	n/a	n/a
20	CTCF	chr7:39453943-39454289	GM12878	blood:	n/a	n/a
21	CTCF	chr7:39453840-39453990	BE2_C	brain:	n/a	n/a
22	CTCF	chr7:39453980-39454130	AG10803	skin:	n/a	n/a
23	CTCF	chr7:39453980-39454130	HMEC	breast:	n/a	n/a
24	CTCF	chr7:39453940-39454090	HCM	heart:	n/a	n/a
25	CTCF	chr7:39454000-39454150	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr7:39453980-39454130	HCFaa	heart:	n/a	n/a
27	CTCF	chr7:39433980-39434130	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:39453960-39454110	HAc	cerebellar:	n/a	n/a
29	CTCF	chr7:39454000-39454150	HRE	kidney:	n/a	n/a
30	CTCF	chr7:39454000-39454150	AG04449	skin:	n/a	n/a
31	CTCF	chr7:39454000-39454150	GM12869	blood:	n/a	n/a
32	CTCF	chr7:39434080-39434230	HEK293	kidney:	n/a	n/a
33	CTCF	chr7:39434120-39434270	RPTEC	kidney:	n/a	n/a
34	CTCF	chr7:39439339-39439402	GM13976	blood:	n/a	n/a
35	CTCF	chr7:39453840-39453990	A549	lung:	n/a	n/a
36	CTCF	chr7:39454000-39454150	HCT-116	colon:	n/a	n/a
37	CTCF	chr7:39453980-39454130	BE2_C	brain:	n/a	n/a
38	CTCF	chr7:39454000-39454150	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr7:39453980-39454130	GM12870	blood:	n/a	n/a
40	CTCF	chr7:39446360-39446510	Caco-2	colon:	n/a	n/a
41	CTCF	chr7:39453980-39454130	GM12875	blood:	n/a	n/a
42	CTCF	chr7:39454000-39454150	HepG2	liver:	n/a	n/a
43	CTCF	chr7:39453960-39454110	GM12864	blood:	n/a	n/a
44	CTCF	chr7:39454000-39454150	GM12874	blood:	n/a	n/a
45	CTCF	chr7:39453880-39454030	GM12865	blood:	n/a	n/a
46	CTCF	chr7:39453960-39454110	HRE	kidney:	n/a	n/a
47	CTCF	chr7:39454000-39454150	GM12867	blood:	n/a	n/a
48	CTCF	chr7:39453980-39454130	HPF	lung:	n/a	n/a
49	CTCF	chr7:39453960-39454110	GM12872	blood:	n/a	n/a
50	CTCF	chr7:39454000-39454150	GM12868	blood:	n/a	n/a

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39453855-39453905	MCF10A-Er-Src	breast:	n/a
2	chr7:39453855-39453905	GM19239	blood:	n/a
3	chr7:39453532-39453582	CMK	blood:	n/a
4	chr7:39453855-39453905	AG09309	skin:	n/a
5	chr7:39453855-39453905	MCF10A-Er-Src	breast:	n/a
6	chr7:39453855-39453905	GM19239	blood:	n/a
7	chr7:39453532-39453582	CMK	blood:	n/a
8	chr7:39453855-39453905	AG09309	skin:	n/a
9	chr7:39451576-39451626	NB4	blood:	n/a
10	chr7:39451576-39451626	Hela-S3	cervix:	n/a
11	chr7:39453784-39453834	T-47D	breast:	n/a
12	chr7:39453625-39453675	GM06990	blood:	n/a
13	chr7:39446909-39446959	GM12892	blood:	n/a
14	chr7:39451576-39451626	GM12891	blood:	n/a
15	chr7:39453625-39453675	H1-hESC	embryonic stem cell:	embryo
16	chr7:39453532-39453582	U87	brain:	n/a
17	chr7:39453784-39453834	HL-60	blood:	n/a
18	chr7:39453784-39453834	HRCEpiC	kidney:	n/a
19	chr7:39446909-39446959	H1-hESC	embryonic stem cell:	embryo
20	chr7:39446909-39446959	CMK	blood:	n/a
21	chr7:39453532-39453582	K562	blood:	n/a
22	chr7:39450193-39450243	NH-A	brain:	n/a
23	chr7:39453625-39453675	HAEpiC	amniotic membrane:	n/a
24	chr7:39453704-39453754	MCF-7	breast:	n/a
25	chr7:39451576-39451626	CMK	blood:	n/a
26	chr7:39453855-39453905	HAEpiC	amniotic membrane:	n/a
27	chr7:39446909-39446959	BE2_C	brain:	n/a
28	chr7:39453704-39453754	ECC-1	luminal epithelium:	n/a
29	chr7:39451576-39451626	NH-A	brain:	n/a
30	chr7:39446909-39446959	GM12878	blood:	n/a
31	chr7:39453704-39453754	PrEC	prostate:	n/a
32	chr7:39453784-39453834	CMK	blood:	n/a
33	chr7:39453532-39453582	HRE	kidney:	n/a
34	chr7:39453532-39453582	PANC-1	pancreas:	n/a
35	chr7:39453704-39453754	Hepatocyte	liver:	n/a
36	chr7:39453855-39453905	AG04449	skin:	fetal
37	chr7:39451576-39451626	HMEC	breast:	n/a
38	chr7:39446909-39446959	U87	brain:	n/a
39	chr7:39453855-39453905	SK-N-SH_RA	brain:	n/a
40	chr7:39446909-39446959	Hepatocyte	liver:	n/a
41	chr7:39453704-39453754	SAEC	small airway:	n/a
42	chr7:39450193-39450243	LNCaP	prostate:	n/a
43	chr7:39453784-39453834	HCF	heart:	n/a
44	chr7:39451576-39451626	AG04450	lung:	fetal
45	chr7:39446909-39446959	SK-N-SH_RA	brain:	n/a
46	chr7:39453855-39453905	PrEC	prostate:	n/a
47	chr7:39446909-39446959	BJ	skin:	n/a
48	chr7:39450193-39450243	HEEpiC	esophagus:	n/a
49	chr7:39450193-39450243	SK-N-SH	brain:	n/a
50	chr7:39446909-39446959	HRE	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:39453463..39455969-chr7:39846035..39848815,2	K562	blood:
2	chr7:39432032..39434536-chr7:39435628..39438240,2	K562	blood:
3	chr7:39440359..39443090-chr7:39454354..39455934,2	K562	blood:
4	chr7:39435823..39437973-chr7:39441882..39444304,3	K562	blood:
5	chr7:39435823..39437973-chr7:39441882..39444304,3	K562	blood:
6	chr7:39424668..39427286-chr7:39432218..39433755,2	MCF-7	breast:
7	chr7:39432032..39434536-chr7:39435628..39438240,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VPS41-2	chr7:39445616-39445718	NR_046711
2	lnc-VPS41-2	chr7:39444197-39444382	ENSG00000224122.1
3	lnc-VPS41-2	chr7:39445933-39445945	NR_046711
4	lnc-VPS41-2	chr7:39445616-39445718	ENSG00000224122.1
5	lnc-VPS41-2	chr7:39446035-39446111	NONHSAT120202
6	lnc-VPS41-2	chr7:39444343-39444382	NONHSAT120202
7	lnc-VPS41-2	chr7:39445616-39445728	NONHSAT120202
8	lnc-VPS41-2	chr7:39444526-39444604	NONHSAT120202
9	lnc-VPS41-2	chr7:39444526-39444604	ENSG00000224122.1
10	lnc-VPS41-2	chr7:39444198-39444382	NR_046711
11	lnc-VPS41-2	chr7:39445933-39445945	ENSG00000224122.1
12	lnc-VPS41-2	chr7:39444526-39444604	NR_046711

No data

Variant related genes	Relation type
POU6F2-AS1	TF binding region
POU6F2	TF binding region
POU6F2-AS1	CpG island
POU6F2	CpG island

Extended variants
information (count: 760 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75568349	chr7:39431075-39431076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529758703	chr7:39431089-39431090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368214775	chr7:39431095-39431096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544209118	chr7:39431126-39431127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370304573	chr7:39431206-39431207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561152544	chr7:39431250-39431251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529730286	chr7:39431283-39431284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10256992	chr7:39431315-39431316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566576847	chr7:39431320-39431321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571051118	chr7:39431324-39431325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147349684	chr7:39431445-39431446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376158046	chr7:39431447-39431448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10227915	chr7:39431588-39431589	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs112507249	chr7:39431596-39431597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180727428	chr7:39431665-39431666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571791765	chr7:39431668-39431669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144204258	chr7:39431753-39431754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146627659	chr7:39431790-39431791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557264657	chr7:39431795-39431796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141442826	chr7:39431874-39431875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567582573	chr7:39431943-39431944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536267068	chr7:39432015-39432016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200949824	chr7:39432049-39432050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552900587	chr7:39432054-39432055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547295974	chr7:39432152-39432153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367846882	chr7:39432172-39432173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568478092	chr7:39432195-39432196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185119060	chr7:39432277-39432278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58695218	chr7:39432330-39432331	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs575383067	chr7:39432338-39432339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61105243	chr7:39432434-39432435	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs371622556	chr7:39432437-39432438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571947161	chr7:39432495-39432496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529971365	chr7:39432498-39432499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143332706	chr7:39432558-39432559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61543464	chr7:39432597-39432598	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532132570	chr7:39432606-39432607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552011891	chr7:39432618-39432619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75501318	chr7:39432641-39432642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374627919	chr7:39432642-39432643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558377733	chr7:39432686-39432687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76597358	chr7:39432690-39432691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540961144	chr7:39432714-39432715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536506506	chr7:39432750-39432751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377723726	chr7:39432753-39432754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553241889	chr7:39432845-39432846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189149899	chr7:39432886-39432887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375408428	chr7:39432919-39432920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539008053	chr7:39432953-39432954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558801282	chr7:39432961-39432962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39426000-39432800	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:39431400-39431600	Enhancers	Fetal Muscle Trunk	muscle
3	chr7:39431800-39432200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:39431800-39432200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:39431800-39432400	Enhancers	Fetal Stomach	stomach
6	chr7:39431800-39432600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:39431800-39432800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:39432000-39432200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:39432000-39432400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr7:39432000-39432400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:39432000-39432400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:39432000-39432400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:39432000-39432400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:39432000-39433200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:39432400-39434000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:39432400-39434000	Weak transcription	Fetal Stomach	stomach
17	chr7:39432400-39439600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr7:39432400-39439800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr7:39432800-39433200	Enhancers	Fetal Muscle Leg	muscle
20	chr7:39432800-39433200	Enhancers	HSMMtube	muscle
21	chr7:39433200-39434400	Weak transcription	HSMMtube	muscle
22	chr7:39433200-39439400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr7:39434000-39434200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:39434000-39434200	Enhancers	Fetal Stomach	stomach
25	chr7:39434000-39438800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr7:39434200-39434400	Enhancers	Fetal Kidney	kidney
27	chr7:39434400-39434600	Enhancers	HSMMtube	muscle
28	chr7:39436200-39436400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:39436200-39436800	Enhancers	HSMMtube	muscle
30	chr7:39436400-39445400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:39437600-39446000	Weak transcription	Pancreas	Pancrea
32	chr7:39438800-39441000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:39439400-39441200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:39439600-39440200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:39439600-39440600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:39439600-39440800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr7:39439600-39440800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:39439600-39440800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:39439600-39441600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:39439800-39440000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:39439800-39441000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:39439800-39441000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:39439800-39441400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:39440000-39440800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:39440200-39446000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:39440400-39440800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr7:39440600-39440800	Enhancers	Right Atrium	heart
48	chr7:39440600-39441800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr7:39440800-39446000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr7:39441000-39446000	Weak transcription	H9 Cell Line	embryonic stem cell

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