Variant report

Variant	esv2754040
Chromosome Location	chr7:145303352-145698352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1459)
CpG islands
(count:244)
Chromatin interactive
region (count:124)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:145590937-145591464	K562	blood:	n/a	n/a
2	ARID3A	chr7:145408904-145408999	K562	blood:	n/a	n/a
3	ARID3A	chr7:145652488-145652580	K562	blood:	n/a	n/a
4	ARID3A	chr7:145485347-145485864	K562	blood:	n/a	n/a
5	ARID3A	chr7:145497714-145497729	K562	blood:	n/a	n/a
6	ARID3A	chr7:145481917-145482313	K562	blood:	n/a	n/a
7	ARID3A	chr7:145482518-145483645	K562	blood:	n/a	n/a
8	ARID3A	chr7:145586627-145586723	K562	blood:	n/a	n/a
9	ARID3A	chr7:145677810-145677911	K562	blood:	n/a	n/a
10	ARID3A	chr7:145469579-145469679	K562	blood:	n/a	n/a
11	ARID3A	chr7:145481496-145481708	K562	blood:	n/a	n/a
12	ATF1	chr7:145481543-145482452	K562	blood:	n/a	n/a
13	ATF1	chr7:145591025-145591463	K562	blood:	n/a	n/a
14	ATF1	chr7:145494627-145494891	K562	blood:	n/a	n/a
15	ATF1	chr7:145402350-145402550	K562	blood:	n/a	n/a
16	ATF1	chr7:145571172-145571311	K562	blood:	n/a	n/a
17	ATF3	chr7:145478558-145478823	K562	blood:	n/a	n/a
18	ATF3	chr7:145683356-145683677	K562	blood:	n/a	n/a
19	BACH1	chr7:145604867-145604957	K562	blood:	n/a	n/a
20	BACH1	chr7:145642174-145642233	K562	blood:	n/a	n/a
21	BACH1	chr7:145545784-145545955	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:145574294-145574418	K562	blood:	n/a	n/a
23	BACH1	chr7:145427550-145427571	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:145330626-145330938	K562	blood:	n/a	chr7:145330787-145330801
25	BACH1	chr7:145592553-145592580	K562	blood:	n/a	n/a
26	BACH1	chr7:145686566-145686880	K562	blood:	n/a	n/a
27	BACH1	chr7:145540634-145540638	K562	blood:	n/a	n/a
28	BACH1	chr7:145563102-145563285	K562	blood:	n/a	n/a
29	BACH1	chr7:145560572-145560672	K562	blood:	n/a	n/a
30	BACH1	chr7:145602030-145602238	K562	blood:	n/a	n/a
31	BACH1	chr7:145330643-145330967	H1-hESC	embryonic stem cell:	n/a	chr7:145330787-145330801
32	BACH1	chr7:145559570-145559829	K562	blood:	n/a	n/a
33	BATF	chr7:145694357-145694559	GM12878	blood:	n/a	n/a
34	BATF	chr7:145694359-145694555	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:145694347-145694680	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:145694365-145694584	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:145483925-145484217	K562	blood:	n/a	n/a
38	BHLHE40	chr7:145660449-145660549	K562	blood:	n/a	n/a
39	BHLHE40	chr7:145545900-145546088	K562	blood:	n/a	n/a
40	BHLHE40	chr7:145683463-145683590	K562	blood:	n/a	n/a
41	BHLHE40	chr7:145556309-145556347	K562	blood:	n/a	n/a
42	BHLHE40	chr7:145591010-145591349	K562	blood:	n/a	n/a
43	BHLHE40	chr7:145481403-145482455	K562	blood:	n/a	n/a
44	BHLHE40	chr7:145616543-145616610	K562	blood:	n/a	n/a
45	BHLHE40	chr7:145547311-145547373	K562	blood:	n/a	n/a
46	BHLHE40	chr7:145621411-145621433	K562	blood:	n/a	n/a
47	BHLHE40	chr7:145694345-145694571	HepG2	liver:	n/a	n/a
48	BHLHE40	chr7:145477041-145477292	K562	blood:	n/a	n/a
49	BRCA1	chr7:145421193-145421324	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr7:145545859-145546048	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145396445-145396495	NT2-D1	testis:	n/a
2	chr7:145395722-145395772	HUVEC	blood vessel:	n/a
3	chr7:145395986-145396036	SK-N-SH	brain:	n/a
4	chr7:145689965-145690015	Hepatocyte	liver:	n/a
5	chr7:145689965-145690015	HCF	heart:	n/a
6	chr7:145689965-145690015	SK-N-SH	brain:	n/a
7	chr7:145689965-145690015	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:145395986-145396036	Hela-S3	cervix:	n/a
9	chr7:145395986-145396036	BE2_C	brain:	n/a
10	chr7:145395986-145396036	Hepatocyte	liver:	n/a
11	chr7:145395986-145396036	CMK	blood:	n/a
12	chr7:145396445-145396495	SK-N-MC	brain:	n/a
13	chr7:145396445-145396495	SK-N-SH_RA	brain:	n/a
14	chr7:145689965-145690015	GM19239	blood:	n/a
15	chr7:145395722-145395772	PFSK-1	brain:	n/a
16	chr7:145395986-145396036	LNCaP	prostate:	n/a
17	chr7:145396445-145396495	IMR90	lung:	fetal
18	chr7:145395986-145396036	H1-hESC	embryonic stem cell:	embryo
19	chr7:145396445-145396495	A549	lung:	n/a
20	chr7:145395722-145395772	GM12878	blood:	n/a
21	chr7:145396445-145396495	Hela-S3	cervix:	n/a
22	chr7:145689965-145690015	A549	lung:	n/a
23	chr7:145689965-145690015	HUVEC	blood vessel:	n/a
24	chr7:145396445-145396495	HUVEC	blood vessel:	n/a
25	chr7:145395722-145395772	NT2-D1	testis:	n/a
26	chr7:145395986-145396036	NB4	blood:	n/a
27	chr7:145396445-145396495	PANC-1	pancreas:	n/a
28	chr7:145396445-145396495	HL-60	blood:	n/a
29	chr7:145396445-145396495	AG09319	gingival:	n/a
30	chr7:145689965-145690015	GM12891	blood:	n/a
31	chr7:145395986-145396036	Caco-2	colon:	n/a
32	chr7:145395986-145396036	MCF-7	breast:	n/a
33	chr7:145395722-145395772	HCM	heart:	n/a
34	chr7:145689965-145690015	HEEpiC	esophagus:	n/a
35	chr7:145395722-145395772	ECC-1	luminal epithelium:	n/a
36	chr7:145395722-145395772	MCF10A-Er-Src	breast:	n/a
37	chr7:145395722-145395772	HIPEpiC	eye:	n/a
38	chr7:145395986-145396036	HRCEpiC	kidney:	n/a
39	chr7:145396445-145396495	HCM	heart:	n/a
40	chr7:145395986-145396036	HEK293	kidney:	embryo
41	chr7:145395986-145396036	PANC-1	pancreas:	n/a
42	chr7:145396445-145396495	AG04449	skin:	fetal
43	chr7:145395986-145396036	GM12891	blood:	n/a
44	chr7:145395986-145396036	GM12878	blood:	n/a
45	chr7:145395722-145395772	T-47D	breast:	n/a
46	chr7:145395986-145396036	HIPEpiC	eye:	n/a
47	chr7:145396445-145396495	HIPEpiC	eye:	n/a
48	chr7:145395986-145396036	ECC-1	luminal epithelium:	n/a
49	chr7:145395986-145396036	BJ	skin:	n/a
50	chr7:145395722-145395772	GM12891	blood:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:145449251..145450121-chr7:145786995..145787798,2	K562	blood:
2	chr7:145526235..145528580-chr7:145532723..145534447,2	K562	blood:
3	chr7:145329048..145330913-chr7:145333895..145335425,2	K562	blood:
4	chr7:145623731..145626417-chr7:145628652..145631149,2	K562	blood:
5	chr7:145587469..145590118-chr7:145600376..145602671,2	K562	blood:
6	chr7:145488061..145490636-chr7:145491307..145495492,3	K562	blood:
7	chr7:145393605..145397108-chr7:145398952..145403129,4	K562	blood:
8	chr7:145638170..145640134-chr7:145641870..145644599,2	K562	blood:
9	chr7:145480955..145483168-chr7:145505213..145507964,2	K562	blood:
10	chr7:145496380..145498149-chr7:145531231..145534208,2	K562	blood:
11	chr7:145528361..145531819-chr7:145535311..145538302,3	K562	blood:
12	chr7:145493230..145496717-chr7:145496905..145498900,3	K562	blood:
13	chr7:145581729..145584075-chr7:145587709..145589979,2	K562	blood:
14	chr7:145623731..145626417-chr7:145628652..145631149,2	K562	blood:
15	chr7:145680328..145682466-chr7:145758892..145760742,2	K562	blood:
16	chr7:145691152..145693851-chr7:145700419..145703123,2	K562	blood:
17	chr7:145481226..145483746-chr7:145496053..145497822,2	K562	blood:
18	chr7:145620799..145622783-chr7:145631883..145633696,2	K562	blood:
19	chr7:145693446..145695856-chr7:145705246..145708235,3	K562	blood:
20	chr7:145502354..145504603-chr7:145510015..145512590,2	K562	blood:
21	chr7:145350267..145350911-chr7:145545526..145546232,2	MCF-7	breast:
22	chr7:145490921..145492885-chr7:145501378..145504321,2	K562	blood:
23	chr7:145549363..145550991-chr7:145552735..145554413,2	K562	blood:
24	chr7:145563311..145566227-chr7:145589236..145592014,2	K562	blood:
25	chr7:145496261..145498317-chr7:145500912..145502935,2	K562	blood:
26	chr7:145462169..145465094-chr7:145472169..145474075,2	K562	blood:
27	chr7:145521688..145524428-chr7:145525978..145528243,2	K562	blood:
28	chr7:145633292..145636880-chr7:145639535..145641924,3	K562	blood:
29	chr7:145488061..145490636-chr7:145491307..145495492,3	K562	blood:
30	chr7:145481226..145483746-chr7:145496053..145497822,2	K562	blood:
31	chr7:145688129..145689794-chr7:145691841..145693343,2	K562	blood:
32	chr7:145570273..145573206-chr7:145582083..145584051,2	K562	blood:
33	chr7:145476367..145479131-chr7:145497414..145500253,2	K562	blood:
34	chr7:145340289..145342911-chr7:145343463..145345865,2	K562	blood:
35	chr7:145641024..145642778-chr7:145655488..145657361,2	K562	blood:
36	chr7:145426356..145428524-chr7:145429528..145431932,2	K562	blood:
37	chr7:145581729..145584075-chr7:145587709..145589979,2	K562	blood:
38	chr7:145320589..145323367-chr7:145325718..145327864,2	K562	blood:
39	chr7:145640094..145641820-chr7:145645010..145646727,2	K562	blood:
40	chr7:145528361..145531819-chr7:145535311..145538302,3	K562	blood:
41	chr7:145473213..145476091-chr7:145481669..145483827,2	K562	blood:
42	chr7:145329048..145330913-chr7:145333895..145335425,2	K562	blood:
43	chr7:145480904..145484102-chr7:145498283..145500839,4	K562	blood:
44	chr7:145320589..145323367-chr7:145325718..145327864,2	K562	blood:
45	chr7:145393605..145397108-chr7:145398952..145403129,4	K562	blood:
46	chr7:145496261..145498317-chr7:145500912..145502935,2	K562	blood:
47	chr7:145620799..145622783-chr7:145631883..145633696,2	K562	blood:
48	chr7:145496380..145498149-chr7:145531231..145534208,2	K562	blood:
49	chr7:145679343..145681995-chr7:145683818..145685327,2	K562	blood:
50	chr7:145641024..145642778-chr7:145655488..145657361,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP2-5	chr7:145307444-145307904	expReg_chr7_11793_+
2	lnc-TPK1-1	chr7:145372975-145373385	XLOC_006634
3	lnc-TPK1-1	chr7:145378202-145378462	XLOC_006634

No data

Variant related genes	Relation type
ENSG00000230746	TF binding region
ENSG00000230746	CpG island
ENSG00000230746	chromatin interactions

Extended variants
information (count: 8778 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:8778 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532521466	chr7:145307546-145307547	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs114786528	chr7:145307562-145307563	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs569314108	chr7:145307581-145307582	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs569147662	chr7:145307582-145307583	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs111387465	chr7:145307590-145307591	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs191737506	chr7:145307596-145307597	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs367645150	chr7:145307597-145307598	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs533354967	chr7:145307641-145307642	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs566664298	chr7:145307654-145307655	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs181851911	chr7:145307707-145307708	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs558608908	chr7:145307768-145307769	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs570485722	chr7:145307796-145307797	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs537426318	chr7:145307803-145307804	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs555762438	chr7:145307808-145307809	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs547169609	chr7:145307810-145307811	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs850503	chr7:145307813-145307814	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs538910703	chr7:145307815-145307816	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs555010533	chr7:145307831-145307832	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs547667292	chr7:145307850-145307851	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs573377271	chr7:145307865-145307866	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs73736505	chr7:145307900-145307901	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs139719596	chr7:145320846-145320847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371086819	chr7:145320850-145320851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551710862	chr7:145320867-145320868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570111340	chr7:145320910-145320911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115855290	chr7:145320921-145320922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550977323	chr7:145320961-145320962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569562269	chr7:145321102-145321103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536410163	chr7:145321152-145321153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555210300	chr7:145321154-145321155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566923639	chr7:145321181-145321182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10234759	chr7:145321200-145321201	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs186209111	chr7:145321237-145321238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116802783	chr7:145321259-145321260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148293374	chr7:145321279-145321280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541850515	chr7:145321286-145321287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556153957	chr7:145321293-145321294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79062220	chr7:145321304-145321305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149960176	chr7:145321350-145321351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559921025	chr7:145321357-145321358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12112078	chr7:145321374-145321375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557360159	chr7:145321405-145321406	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545486125	chr7:145321434-145321435	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115092170	chr7:145321510-145321511	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191063027	chr7:145321533-145321534	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79238258	chr7:145321592-145321593	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142328514	chr7:145321611-145321612	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530420899	chr7:145321619-145321620	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548945654	chr7:145321621-145321622	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547329844	chr7:145321680-145321681	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145320800-145321400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr7:145321200-145322600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:145321400-145322000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:145322000-145322800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:145332600-145333000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr7:145340600-145341000	Enhancers	Hela-S3	cervix
7	chr7:145340800-145342200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:145341000-145341200	Flanking Active TSS	Hela-S3	cervix
9	chr7:145341200-145342400	Active TSS	Hela-S3	cervix
10	chr7:145342200-145343400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:145342400-145342600	Flanking Active TSS	Hela-S3	cervix
12	chr7:145343400-145344200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:145362000-145362200	Enhancers	Fetal Lung	lung
14	chr7:145362000-145363400	Enhancers	Fetal Stomach	stomach
15	chr7:145362000-145365000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:145362200-145366000	Weak transcription	Fetal Lung	lung
17	chr7:145362400-145363400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr7:145366600-145367000	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr7:145366800-145367000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:145371600-145372600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:145373000-145373400	Active TSS	Right Atrium	heart
22	chr7:145373400-145375000	Weak transcription	Right Atrium	heart
23	chr7:145374600-145375200	Active TSS	Stomach Smooth Muscle	stomach
24	chr7:145375000-145378600	Active TSS	Right Atrium	heart
25	chr7:145375200-145375800	Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr7:145375200-145377000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr7:145377000-145378200	Active TSS	Stomach Smooth Muscle	stomach
28	chr7:145389000-145390000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:145389400-145389800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:145389400-145390400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:145389400-145390600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:145389600-145389800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:145389600-145390000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:145389600-145390600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:145389600-145390600	Enhancers	Placenta Amnion	Placenta Amnion
36	chr7:145389800-145390200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr7:145389800-145390200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:145389800-145394400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:145390400-145393000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:145390600-145393200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:145393000-145394000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:145393200-145394000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:145393800-145395600	Active TSS	K562	blood
44	chr7:145394400-145394600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:145395800-145396200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:145410200-145410400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:145410400-145415200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:145413200-145413400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr7:145413400-145413600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr7:145413400-145413600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links