Variant report

Variant	esv3445290
Chromosome Location	chr7:99868266-99870664
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	chr7:99868232-99868445	HepG2	liver:	n/a	n/a
2	ATF3	chr7:99869654-99870002	K562	blood:	n/a	chr7:99869812-99869821
3	BACH1	chr7:99869775-99869955	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr7:99869393-99869661	GM12878	blood:	n/a	n/a
5	BCL3	chr7:99869522-99870148	GM12878	blood:	n/a	chr7:99869953-99869966 chr7:99869950-99869963 chr7:99869957-99869970
6	BCL3	chr7:99869668-99870102	A549	lung:	n/a	chr7:99869953-99869966 chr7:99869950-99869963 chr7:99869957-99869970
7	BCLAF1	chr7:99869609-99869956	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:99869780-99870096	K562	blood:	n/a	chr7:99869947-99869963 chr7:99869956-99869972 chr7:99869950-99869966 chr7:99869813-99869829 chr7:99869953-99869969
9	BHLHE40	chr7:99869842-99870008	GM12878	blood:	n/a	chr7:99869947-99869963 chr7:99869956-99869972 chr7:99869950-99869966 chr7:99869953-99869969
10	CBX3	chr7:99869687-99870331	K562	blood:	n/a	n/a
11	CCNT2	chr7:99869613-99870080	K562	blood:	n/a	n/a
12	CEBPB	chr7:99869760-99869964	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr7:99869821-99870103	HepG2	liver:	n/a	n/a
14	CHD1	chr7:99869858-99870003	GM12878	blood:	n/a	n/a
15	CHD2	chr7:99869757-99869958	GM12878	blood:	n/a	chr7:99869813-99869823
16	CHD2	chr7:99869750-99870051	Hela-S3	cervix:	n/a	chr7:99869813-99869823
17	CREB1	chr7:99869593-99870103	A549	lung:	n/a	n/a
18	CTCF	chr7:99869900-99870050	GM12878	blood:	n/a	n/a
19	CTCF	chr7:99869217-99870250	K562	blood:	n/a	chr7:99869431-99869444
20	CTCF	chr7:99869422-99869486	GM19238	blood:	n/a	chr7:99869431-99869444
21	CTCF	chr7:99869800-99869950	HCT-116	colon:	n/a	n/a
22	CTCF	chr7:99869940-99870090	GM12865	blood:	n/a	n/a
23	CTCF	chr7:99869880-99870030	A549	lung:	n/a	n/a
24	CTCF	chr7:99869320-99869470	GM12871	blood:	n/a	chr7:99869431-99869444
25	CTCF	chr7:99869360-99869510	SAEC	small airway:	n/a	chr7:99869431-99869444
26	CTCF	chr7:99869880-99870030	GM12871	blood:	n/a	n/a
27	CTCF	chr7:99868580-99868730	HFF	foreskin:	n/a	n/a
28	CTCF	chr7:99869360-99869510	NB4	blood:	n/a	chr7:99869431-99869444
29	CTCF	chr7:99869869-99870145	GM13977	blood:	n/a	n/a
30	CTCF	chr7:99869747-99870141	K562	blood:	n/a	n/a
31	CTCF	chr7:99869860-99870010	NHLF	lung:	n/a	n/a
32	CTCF	chr7:99869360-99869510	GM12867	blood:	n/a	chr7:99869431-99869444
33	CTCF	chr7:99869900-99870050	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr7:99869840-99869990	HFF	foreskin:	n/a	n/a
35	CTCF	chr7:99869878-99870024	A549	lung:	n/a	n/a
36	CTCF	chr7:99869360-99869510	AG04449	skin:	n/a	chr7:99869431-99869444
37	CTCF	chr7:99869860-99870010	GM12869	blood:	n/a	n/a
38	CTCF	chr7:99869900-99870050	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:99869880-99870030	GM12868	blood:	n/a	n/a
40	CTCF	chr7:99869840-99869990	HVMF	connective:	n/a	n/a
41	CTCF	chr7:99869880-99870030	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr7:99868240-99868390	AG04449	skin:	n/a	n/a
43	CTCF	chr7:99869806-99870053	GM19239	blood:	n/a	n/a
44	CTCF	chr7:99869980-99870130	GM12864	blood:	n/a	n/a
45	CTCF	chr7:99868260-99868410	HFF	foreskin:	n/a	n/a
46	CTCF	chr7:99869900-99870050	AG09319	gingival:	n/a	n/a
47	CTCF	chr7:99869860-99870010	SAEC	small airway:	n/a	n/a
48	CTCF	chr7:99869360-99869510	K562	blood:	n/a	chr7:99869431-99869444
49	CTCF	chr7:99869483-99869542	GM10248	blood:	n/a	n/a
50	CTCF	chr7:99870119-99870127	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99869835-99869885	LNCaP	prostate:	n/a
2	chr7:99869835-99869885	LNCaP	prostate:	n/a
3	chr7:99870040-99870090	GM12878	blood:	n/a
4	chr7:99869529-99869579	SK-N-MC	brain:	n/a
5	chr7:99870057-99870107	NT2-D1	testis:	n/a
6	chr7:99870040-99870090	AG09319	gingival:	n/a
7	chr7:99869454-99869504	Hepatocyte	liver:	n/a
8	chr7:99869529-99869579	AG09319	gingival:	n/a
9	chr7:99869835-99869885	NT2-D1	testis:	n/a
10	chr7:99870057-99870107	BJ	skin:	n/a
11	chr7:99869529-99869579	AoSMC	blood vessel:	n/a
12	chr7:99869454-99869504	MCF-7	breast:	n/a
13	chr7:99869784-99869834	AG04449	skin:	fetal
14	chr7:99870147-99870197	HCM	heart:	n/a
15	chr7:99870040-99870090	HCT-116	colon:	n/a
16	chr7:99869835-99869885	NHDF-neo	bronchial:	n/a
17	chr7:99869529-99869579	GM12891	blood:	n/a
18	chr7:99869454-99869504	GM12892	blood:	n/a
19	chr7:99869454-99869504	HCT-116	colon:	n/a
20	chr7:99870182-99870232	PrEC	prostate:	n/a
21	chr7:99869835-99869885	HEK293	kidney:	embryo
22	chr7:99869529-99869579	SKMC	muscle:	n/a
23	chr7:99869028-99869078	H1-hESC	embryonic stem cell:	embryo
24	chr7:99870147-99870197	SK-N-SH_RA	brain:	n/a
25	chr7:99869835-99869885	AG09309	skin:	n/a
26	chr7:99869454-99869504	AG04449	skin:	fetal
27	chr7:99870147-99870197	ovcar-3	ovarian:	n/a
28	chr7:99869454-99869504	GM06990	blood:	n/a
29	chr7:99870147-99870197	Caco-2	colon:	n/a
30	chr7:99870147-99870197	GM12878	blood:	n/a
31	chr7:99870182-99870232	K562	blood:	n/a
32	chr7:99869784-99869834	HCPEpiC	choroid plexus:	n/a
33	chr7:99870057-99870107	MCF-7	breast:	n/a
34	chr7:99870147-99870197	HMEC	breast:	n/a
35	chr7:99869784-99869834	NT2-D1	testis:	n/a
36	chr7:99870182-99870232	HepG2	liver:	n/a
37	chr7:99869028-99869078	U87	brain:	n/a
38	chr7:99869529-99869579	K562	blood:	n/a
39	chr7:99869835-99869885	HUVEC	blood vessel:	n/a
40	chr7:99870057-99870107	HMEC	breast:	n/a
41	chr7:99869529-99869579	HEK293	kidney:	embryo
42	chr7:99870040-99870090	HRPEpiC	eye:	n/a
43	chr7:99869028-99869078	AG09309	skin:	n/a
44	chr7:99870057-99870107	MCF10A-Er-Src	breast:	n/a
45	chr7:99869529-99869579	SAEC	small airway:	n/a
46	chr7:99869454-99869504	HNPCEpiC	eye:	n/a
47	chr7:99869454-99869504	Caco-2	colon:	n/a
48	chr7:99870147-99870197	CMK	blood:	n/a
49	chr7:99870182-99870232	HMEC	breast:	n/a
50	chr7:99869454-99869504	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:99746174..99748056-chr7:99869608..99872452,2	K562	blood:
2	chr7:99678858..99680502-chr7:99868393..99870017,2	K562	blood:

Variant related genes	Relation type
ENSG00000239521	TF binding region
GATS	TF binding region
ENSG00000239521	CpG island
GATS	CpG island
ENSG00000188186	chromatin interactions
ENSG00000166526	chromatin interactions

Extended variants
information (count: 74 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544255889	chr7:99868336-99868337	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs12113906	chr7:99868412-99868413	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs577680606	chr7:99868427-99868428	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544799335	chr7:99868446-99868447	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185219311	chr7:99868535-99868536	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112043149	chr7:99868556-99868557	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141233430	chr7:99868574-99868575	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190148579	chr7:99868575-99868576	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552199161	chr7:99868681-99868682	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs371939062	chr7:99868684-99868685	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182379594	chr7:99868690-99868691	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570502007	chr7:99868691-99868692	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565514191	chr7:99868695-99868696	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374127840	chr7:99868727-99868728	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112384309	chr7:99868800-99868801	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531868542	chr7:99868808-99868809	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550025200	chr7:99868876-99868877	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571328899	chr7:99868882-99868883	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538975022	chr7:99868962-99868963	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547582882	chr7:99869065-99869066	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs375646321	chr7:99869140-99869141	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566152328	chr7:99869190-99869191	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13234011	chr7:99869192-99869193	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533791128	chr7:99869252-99869253	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs13234110	chr7:99869259-99869260	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs4084978	chr7:99869268-99869269	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555581711	chr7:99869269-99869270	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs574020730	chr7:99869289-99869290	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs13234340	chr7:99869375-99869376	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538157829	chr7:99869389-99869390	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200171016	chr7:99869446-99869447	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs3735244	chr7:99869455-99869456	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368589202	chr7:99869456-99869457	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372345895	chr7:99869465-99869466	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544948862	chr7:99869502-99869503	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376366977	chr7:99869513-99869514	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368369600	chr7:99869520-99869521	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs371961029	chr7:99869551-99869552	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs376811492	chr7:99869568-99869569	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199808373	chr7:99869589-99869590	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572105615	chr7:99869590-99869591	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs369388870	chr7:99869595-99869596	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373123333	chr7:99869597-99869598	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542885823	chr7:99869600-99869601	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs376626284	chr7:99869609-99869610	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs35408185	chr7:99869655-99869656	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs9692044	chr7:99869678-99869679	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs563824828	chr7:99869766-99869767	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs531762160	chr7:99869776-99869777	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs551246820	chr7:99869790-99869791	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99833000-99868600	Weak transcription	Primary T cells from cord blood	blood
2	chr7:99833200-99868600	Weak transcription	Thymus	Thymus
3	chr7:99842000-99868400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr7:99846400-99868800	Weak transcription	Right Ventricle	heart
5	chr7:99851800-99868400	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr7:99852600-99868400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr7:99853400-99868400	Weak transcription	Primary B cells from cord blood	blood
8	chr7:99858400-99868400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr7:99859000-99868400	Weak transcription	Esophagus	oesophagus
10	chr7:99861400-99868400	Enhancers	Placenta	Placenta
11	chr7:99862800-99869200	Weak transcription	Lung	lung
12	chr7:99863000-99868400	Weak transcription	NHEK	skin
13	chr7:99864600-99868400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr7:99864600-99868600	Weak transcription	Primary B cells from peripheral blood	blood
15	chr7:99865000-99869400	Weak transcription	Spleen	Spleen
16	chr7:99866800-99868400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:99866800-99868600	Enhancers	Fetal Stomach	stomach
18	chr7:99866800-99870600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:99867000-99868800	Flanking Active TSS	Hela-S3	cervix
20	chr7:99867200-99868400	Enhancers	Fetal Muscle Trunk	muscle
21	chr7:99867200-99868800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:99867200-99869000	Enhancers	Stomach Mucosa	stomach
23	chr7:99867400-99868400	Enhancers	HMEC	breast
24	chr7:99867400-99868600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr7:99867400-99868600	Enhancers	K562	blood
26	chr7:99867400-99868800	Enhancers	Fetal Lung	lung
27	chr7:99867400-99870000	Active TSS	Brain Germinal Matrix	brain
28	chr7:99867400-99870200	Active TSS	Rectal Smooth Muscle	rectum
29	chr7:99867400-99870200	Active TSS	HepG2	liver
30	chr7:99867600-99868400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr7:99867600-99868400	Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr7:99867600-99868400	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:99867600-99868800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:99867600-99870000	Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr7:99867600-99870200	Active TSS	Brain Cingulate Gyrus	brain
36	chr7:99867600-99870200	Active TSS	Brain Hippocampus Middle	brain
37	chr7:99867600-99870200	Active TSS	Brain Substantia Nigra	brain
38	chr7:99867600-99870400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:99867600-99870400	Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr7:99867600-99870400	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr7:99867600-99870400	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr7:99867600-99870400	Active TSS	Fetal Brain Female	brain
43	chr7:99867600-99870600	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr7:99867600-99870600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:99867800-99868400	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr7:99867800-99868400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:99867800-99868400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:99867800-99868400	Enhancers	Left Ventricle	heart
49	chr7:99867800-99868800	Enhancers	Liver	Liver
50	chr7:99867800-99868800	Enhancers	Colonic Mucosa	Colon

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