Variant report

Variant	esv2758614
Chromosome Location	chr7:109409980-109607619
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	ATF1	chr7:109521886-109521936	K562	blood:	n/a	n/a
2	BACH1	chr7:109574018-109574056	K562	blood:	n/a	n/a
3	BACH1	chr7:109590985-109591005	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr7:109600731-109601037	K562	blood:	n/a	chr7:109600899-109600910
5	CEBPB	chr7:109515957-109516263	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr7:109596973-109597531	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr7:109519435-109519883	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr7:109595794-109595902	A549	lung:	n/a	n/a
9	CEBPB	chr7:109569232-109569428	A549	lung:	n/a	chr7:109569324-109569333 chr7:109569324-109569333 chr7:109569324-109569333
10	CEBPB	chr7:109519504-109519898	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr7:109569274-109569479	HepG2	liver:	n/a	chr7:109569324-109569333 chr7:109569324-109569333 chr7:109569324-109569333
12	CEBPB	chr7:109515974-109516243	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:109516459-109516657	HepG2	liver:	n/a	chr7:109516631-109516644
14	CEBPB	chr7:109519554-109519767	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:109489562-109489814	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:109600727-109601032	IMR90	lung:	n/a	chr7:109600899-109600910
17	CEBPB	chr7:109422895-109423105	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:109600756-109601006	HepG2	liver:	n/a	chr7:109600899-109600910
19	CEBPB	chr7:109541285-109542360	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:109533050-109533664	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:109510704-109510822	HepG2	liver:	n/a	chr7:109510765-109510776
22	CTCF	chr7:109484280-109484430	GM12873	blood:	n/a	n/a
23	CTCF	chr7:109484540-109484690	RPTEC	kidney:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
24	CTCF	chr7:109484521-109484716	MCF-7	breast:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
25	CTCF	chr7:109484460-109484610	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr7:109484540-109484690	HBMEC	blood vessel:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
27	CTCF	chr7:109484540-109484690	AG04449	skin:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
28	CTCF	chr7:109484540-109484690	WI-38	lung:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
29	CTCF	chr7:109484540-109484690	HRPEpiC	eye:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
30	CTCF	chr7:109484241-109485037	SK-N-SH	brain:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
31	CTCF	chr7:109484560-109484710	HCPEpiC	choroid plexus:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
32	CTCF	chr7:109484520-109484670	Caco-2	colon:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
33	CTCF	chr7:109484596-109484631	A549	lung:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
34	CTCF	chr7:109508040-109508190	GM12871	blood:	n/a	n/a
35	CTCF	chr7:109484540-109484690	HEK293	kidney:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
36	CTCF	chr7:109484560-109484710	GM06990	blood:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
37	CTCF	chr7:109484520-109484670	HRPEpiC	eye:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
38	CTCF	chr7:109606520-109606670	NB4	blood:	n/a	n/a
39	CTCF	chr7:109484580-109484730	WERI-Rb-1	eye:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
40	CTCF	chr7:109508375-109508544	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:109527417-109527468	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:109484500-109484650	GM12865	blood:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
43	CTCF	chr7:109484480-109484630	NHEK	skin:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
44	CTCF	chr7:109484498-109484721	LNCaP	prostate:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
45	CTCF	chr7:109484580-109484730	HEK293	kidney:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
46	CTCF	chr7:109508460-109508610	BE2_C	brain:	n/a	n/a
47	CTCF	chr7:109484503-109484703	SK-N-SH_RA	brain:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
48	CTCF	chr7:109484600-109484750	AG04450	lung:	n/a	chr7:109484609-109484619 chr7:109484604-109484622 chr7:109484607-109484620 chr7:109484606-109484627
49	CTCF	chr7:109424302-109424428	GM13977	blood:	n/a	n/a
50	CTCF	chr7:109441320-109441406	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:109600399-109600449	GM12878	blood:	n/a
2	chr7:109599644-109599694	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:109600733-109600783	MCF10A-Er-Src	breast:	n/a
4	chr7:109600399-109600449	HCT-116	colon:	n/a
5	chr7:109596752-109596802	AoSMC	blood vessel:	n/a
6	chr7:109599644-109599694	AoSMC	blood vessel:	n/a
7	chr7:109599644-109599694	HL-60	blood:	n/a
8	chr7:109585055-109585105	GM19239	blood:	n/a
9	chr7:109600591-109600641	SK-N-SH_RA	brain:	n/a
10	chr7:109600733-109600783	AG04449	skin:	fetal
11	chr7:109570287-109570337	A549	lung:	n/a
12	chr7:109585055-109585105	Hepatocyte	liver:	n/a
13	chr7:109596752-109596802	H1-hESC	embryonic stem cell:	embryo
14	chr7:109485219-109485269	ProgFib	skin:	n/a
15	chr7:109600591-109600641	HCPEpiC	choroid plexus:	n/a
16	chr7:109600591-109600641	GM12878	blood:	n/a
17	chr7:109599644-109599694	HCPEpiC	choroid plexus:	n/a
18	chr7:109600591-109600641	GM12892	blood:	n/a
19	chr7:109600425-109600475	NHDF-neo	bronchial:	n/a
20	chr7:109596752-109596802	PANC-1	pancreas:	n/a
21	chr7:109600399-109600449	AoSMC	blood vessel:	n/a
22	chr7:109600425-109600475	Hepatocyte	liver:	n/a
23	chr7:109570287-109570337	HNPCEpiC	eye:	n/a
24	chr7:109600425-109600475	LNCaP	prostate:	n/a
25	chr7:109485219-109485269	ovcar-3	ovarian:	n/a
26	chr7:109599644-109599694	BE2_C	brain:	n/a
27	chr7:109600591-109600641	BJ	skin:	n/a
28	chr7:109600425-109600475	GM06990	blood:	n/a
29	chr7:109600733-109600783	SKMC	muscle:	n/a
30	chr7:109600399-109600449	HMEC	breast:	n/a
31	chr7:109600591-109600641	SAEC	small airway:	n/a
32	chr7:109485219-109485269	BE2_C	brain:	n/a
33	chr7:109600399-109600449	IMR90	lung:	fetal
34	chr7:109600399-109600449	HRPEpiC	eye:	n/a
35	chr7:109600425-109600475	HUVEC	blood vessel:	n/a
36	chr7:109600733-109600783	NT2-D1	testis:	n/a
37	chr7:109570287-109570337	HIPEpiC	eye:	n/a
38	chr7:109596752-109596802	HUVEC	blood vessel:	n/a
39	chr7:109570287-109570337	ProgFib	skin:	n/a
40	chr7:109600399-109600449	HIPEpiC	eye:	n/a
41	chr7:109600733-109600783	HEK293	kidney:	embryo
42	chr7:109599644-109599694	SKMC	muscle:	n/a
43	chr7:109600399-109600449	T-47D	breast:	n/a
44	chr7:109600425-109600475	K562	blood:	n/a
45	chr7:109600399-109600449	Jurkat	blood:	n/a
46	chr7:109585055-109585105	HUVEC	blood vessel:	n/a
47	chr7:109485219-109485269	HRE	kidney:	n/a
48	chr7:109600399-109600449	MCF-7	breast:	n/a
49	chr7:109600733-109600783	SK-N-MC	brain:	n/a
50	chr7:109570287-109570337	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:109595389..109597303-chr7:109602363..109605295,2	K562	blood:
2	chr12:95693010..95693732-chr7:109461830..109462660,2	MCF-7	breast:
3	chr7:109538440..109540413-chr7:109541881..109544620,2	K562	blood:
4	chr7:109484123..109484950-chr7:110082483..110082993,2	MCF-7	breast:
5	chr7:109537859..109540413-chr7:109543120..109545714,2	K562	blood:
6	chr12:7073001..7074519-chr7:109591479..109593234,2	MCF-7	breast:
7	chr7:109568885..109571688-chr7:109572507..109574918,2	K562	blood:
8	chr7:109524189..109525857-chr7:109531930..109534908,2	K562	blood:
9	chr7:109538440..109540413-chr7:109541881..109544620,2	K562	blood:
10	chr7:109524189..109525857-chr7:109531930..109534908,2	K562	blood:
11	chr7:109484230..109484803-chr7:109844371..109845272,2	MCF-7	breast:
12	chr7:109452833..109454349-chr7:109467899..109470407,2	K562	blood:
13	chr7:109452833..109454349-chr7:109467899..109470407,2	K562	blood:
14	chr20:54797543..54800025-chr7:109465690..109468488,2	MCF-7	breast:
15	chr2:78150104..78151070-chr7:109526792..109527641,2	MCF-7	breast:
16	chr7:109537859..109540413-chr7:109543120..109545714,2	K562	blood:
17	chr7:109568885..109571688-chr7:109572507..109574918,2	K562	blood:
18	chr7:109119620..109121051-chr7:109484305..109485142,3	MCF-7	breast:
19	chr7:109595389..109597303-chr7:109602363..109605295,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMMP2L-8	chr7:109599284-109600270	NR_003024

Variant related genes	Relation type
EIF3IP1	TF binding region
EIF3IP1	CpG island
ENSG00000207708	chromatin interactions
ENSG00000271969	chromatin interactions

Extended variants
information (count: 2699 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2699 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376351584	chr7:109410013-109410014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35999190	chr7:109410084-109410085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532340068	chr7:109410122-109410123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148457029	chr7:109410163-109410164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144095841	chr7:109410164-109410165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188480188	chr7:109410180-109410181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370727145	chr7:109410187-109410188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200154160	chr7:109410285-109410286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528474573	chr7:109410296-109410297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575716315	chr7:109410297-109410298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570121303	chr7:109410304-109410305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531144425	chr7:109410305-109410306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181280167	chr7:109410306-109410307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141099697	chr7:109410404-109410405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550723955	chr7:109410462-109410463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144853196	chr7:109410472-109410473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371321305	chr7:109410473-109410474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs151147051	chr7:109410479-109410480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555425082	chr7:109410480-109410481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140050131	chr7:109410521-109410522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568120447	chr7:109410555-109410556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544236672	chr7:109410622-109410623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185565662	chr7:109410624-109410625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577835204	chr7:109410644-109410645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546046069	chr7:109410648-109410649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373239189	chr7:109410707-109410708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569261814	chr7:109410722-109410723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73191835	chr7:109410828-109410829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182917444	chr7:109410908-109410909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187202507	chr7:109410925-109410926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562051642	chr7:109410947-109410948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530764652	chr7:109410948-109410949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550581396	chr7:109410959-109410960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570574504	chr7:109410961-109410962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs386716767	chr7:109410973-109410974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533233236	chr7:109410994-109410995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373883457	chr7:109411080-109411081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368084996	chr7:109411093-109411094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536141172	chr7:109411138-109411139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150324360	chr7:109411154-109411155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535332417	chr7:109411166-109411167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374881811	chr7:109411187-109411188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555597489	chr7:109411209-109411210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569177002	chr7:109411234-109411235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs117425967	chr7:109411250-109411251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs137979369	chr7:109411259-109411260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62478937	chr7:109411285-109411286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192134331	chr7:109411298-109411299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540320033	chr7:109411332-109411333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182823733	chr7:109411351-109411352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109408800-109410400	Weak transcription	Dnd41	blood
2	chr7:109410400-109410800	Enhancers	Dnd41	blood
3	chr7:109410800-109412400	Weak transcription	Dnd41	blood
4	chr7:109412200-109412800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:109412400-109412600	Enhancers	Dnd41	blood
6	chr7:109412400-109412800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr7:109412400-109413200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:109415600-109416800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:109419400-109419600	Enhancers	Dnd41	blood
10	chr7:109419600-109420600	Weak transcription	Dnd41	blood
11	chr7:109420600-109422600	Enhancers	Dnd41	blood
12	chr7:109422600-109422800	Flanking Active TSS	Dnd41	blood
13	chr7:109422800-109423000	Enhancers	Dnd41	blood
14	chr7:109423000-109423200	Flanking Active TSS	Dnd41	blood
15	chr7:109423200-109425600	Enhancers	Dnd41	blood
16	chr7:109434600-109435200	ZNF genes & repeats	Dnd41	blood
17	chr7:109435000-109435400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:109435200-109435800	Weak transcription	Dnd41	blood
19	chr7:109435800-109436000	Enhancers	Dnd41	blood
20	chr7:109463000-109463600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:109463200-109463600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr7:109465600-109466800	ZNF genes & repeats	Dnd41	blood
23	chr7:109466800-109467000	Enhancers	Dnd41	blood
24	chr7:109474200-109474400	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr7:109482000-109484000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:109482800-109485600	Enhancers	Dnd41	blood
27	chr7:109483600-109483800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:109483800-109484800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:109484200-109485200	Enhancers	A549	lung
30	chr7:109484600-109485600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr7:109484800-109485600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:109484800-109485800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr7:109485000-109485200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr7:109485000-109485600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:109485000-109485600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:109485000-109485600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr7:109485000-109485600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr7:109485000-109485800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr7:109486800-109489200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:109489200-109489400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr7:109489400-109493400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr7:109504000-109504600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:109504200-109504600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr7:109504200-109504800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:109504200-109504800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:109504200-109504800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:109504200-109504800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:109504200-109504800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr7:109504200-109504800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:109504200-109505000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links