Variant report

Variant	nsv961454
Chromosome Location	chr2:96677855-96701857
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	BHLHE40	chr2:96688621-96688761	K562	blood:	n/a	n/a
2	BRCA1	chr2:96688571-96688776	GM12878	blood:	n/a	n/a
3	CTCF	chr2:96688560-96688710	HepG2	liver:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
4	CTCF	chr2:96688511-96688769	GM13977	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
5	CTCF	chr2:96688560-96688710	GM12878	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
6	CTCF	chr2:96678800-96678950	MCF-7	breast:	n/a	chr2:96678808-96678821
7	CTCF	chr2:96688511-96688781	A549	lung:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
8	CTCF	chr2:96688040-96688190	AG10803	skin:	n/a	n/a
9	CTCF	chr2:96688560-96688710	HRE	kidney:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
10	CTCF	chr2:96688540-96688690	GM12869	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
11	CTCF	chr2:96688494-96688787	GM19240	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
12	CTCF	chr2:96699999-96700107	GM12891	blood:	n/a	n/a
13	CTCF	chr2:96690437-96690581	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:96678720-96678870	HA-sp	spinal cord:	n/a	chr2:96678808-96678821
15	CTCF	chr2:96688522-96688771	MCF-7	breast:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
16	CTCF	chr2:96688540-96688690	NB4	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
17	CTCF	chr2:96690473-96690566	K562	blood:	n/a	n/a
18	CTCF	chr2:96688580-96688730	GM12865	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
19	CTCF	chr2:96688560-96688710	GM12874	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
20	CTCF	chr2:96688580-96688730	AG09309	skin:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
21	CTCF	chr2:96688520-96688670	HVMF	connective:	n/a	chr2:96688635-96688648 chr2:96688632-96688650
22	CTCF	chr2:96678780-96678930	A549	lung:	n/a	chr2:96678808-96678821
23	CTCF	chr2:96689040-96689190	GM12874	blood:	n/a	n/a
24	CTCF	chr2:96688560-96688710	HCPEpiC	choroid plexus:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
25	CTCF	chr2:96700108-96700110	GM12891	blood:	n/a	n/a
26	CTCF	chr2:96688474-96688723	ECC-1	luminal epithelium:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
27	CTCF	chr2:96678712-96678915	K562	blood:	n/a	chr2:96678808-96678821
28	CTCF	chr2:96678780-96678930	GM12872	blood:	n/a	chr2:96678808-96678821
29	CTCF	chr2:96688497-96688792	K562	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
30	CTCF	chr2:96688560-96688710	GM12801	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
31	CTCF	chr2:96699867-96699935	GM10266	blood:	n/a	n/a
32	CTCF	chr2:96688503-96688796	GM12878	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
33	CTCF	chr2:96688147-96688799	SK-N-SH	brain:	n/a	chr2:96688671-96688684 chr2:96688385-96688406 chr2:96688635-96688648 chr2:96688632-96688650
34	CTCF	chr2:96688431-96688831	GM12878	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
35	CTCF	chr2:96678793-96678830	HepG2	liver:	n/a	chr2:96678808-96678821
36	CTCF	chr2:96688500-96688650	HVMF	connective:	n/a	chr2:96688635-96688648 chr2:96688632-96688650
37	CTCF	chr2:96688506-96688792	Gliobla	brain:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
38	CTCF	chr2:96699827-96700055	A549	lung:	n/a	n/a
39	CTCF	chr2:96688530-96688763	ProgFib	skin:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
40	CTCF	chr2:96690369-96690639	K562	blood:	n/a	n/a
41	CTCF	chr2:96688540-96688690	GM06990	blood:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
42	CTCF	chr2:96688560-96688710	HUVEC	blood vessel:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
43	CTCF	chr2:96689000-96689150	HepG2	liver:	n/a	n/a
44	CTCF	chr2:96699738-96700092	A549	lung:	n/a	n/a
45	CTCF	chr2:96695011-96695074	Lung_OC	lung:	n/a	n/a
46	CTCF	chr2:96688524-96688778	H1-hESC	embryonic stem cell:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
47	CTCF	chr2:96688560-96688710	NHEK	skin:	n/a	chr2:96688671-96688684 chr2:96688635-96688648 chr2:96688632-96688650
48	CTCF	chr2:96699573-96699665	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr2:96699811-96699999	LNCaP	prostate:	n/a	n/a
50	CTCF	chr2:96699772-96700008	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96679346-96679396	GM19239	blood:	n/a
2	chr2:96679346-96679396	GM19239	blood:	n/a
3	chr2:96689067-96689117	NHDF-neo	bronchial:	n/a
4	chr2:96679346-96679396	HCT-116	colon:	n/a
5	chr2:96679346-96679396	MCF10A-Er-Src	breast:	n/a
6	chr2:96689067-96689117	GM12878	blood:	n/a
7	chr2:96679346-96679396	SK-N-SH	brain:	n/a
8	chr2:96679346-96679396	Caco-2	colon:	n/a
9	chr2:96678476-96678526	LNCaP	prostate:	n/a
10	chr2:96679346-96679396	HL-60	blood:	n/a
11	chr2:96689067-96689117	A549	lung:	n/a
12	chr2:96679346-96679396	K562	blood:	n/a
13	chr2:96678476-96678526	PFSK-1	brain:	n/a
14	chr2:96689067-96689117	GM12891	blood:	n/a
15	chr2:96679346-96679396	HEEpiC	esophagus:	n/a
16	chr2:96679346-96679396	HMEC	breast:	n/a
17	chr2:96678476-96678526	NH-A	brain:	n/a
18	chr2:96679346-96679396	Hepatocyte	liver:	n/a
19	chr2:96679346-96679396	HEK293	kidney:	embryo
20	chr2:96678476-96678526	HCM	heart:	n/a
21	chr2:96678476-96678526	HCF	heart:	n/a
22	chr2:96679346-96679396	HRPEpiC	eye:	n/a
23	chr2:96689067-96689117	HCF	heart:	n/a
24	chr2:96689067-96689117	H1-hESC	embryonic stem cell:	embryo
25	chr2:96689067-96689117	SKMC	muscle:	n/a
26	chr2:96689067-96689117	HUVEC	blood vessel:	n/a
27	chr2:96689067-96689117	HNPCEpiC	eye:	n/a
28	chr2:96689067-96689117	NHBE	bronchial:	n/a
29	chr2:96689067-96689117	SK-N-SH_RA	brain:	n/a
30	chr2:96678476-96678526	MCF-7	breast:	n/a
31	chr2:96689067-96689117	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:96679346-96679396	HIPEpiC	eye:	n/a
33	chr2:96679346-96679396	BJ	skin:	n/a
34	chr2:96689067-96689117	NB4	blood:	n/a
35	chr2:96678476-96678526	CMK	blood:	n/a
36	chr2:96689067-96689117	ProgFib	skin:	n/a
37	chr2:96678476-96678526	Hepatocyte	liver:	n/a
38	chr2:96679346-96679396	T-47D	breast:	n/a
39	chr2:96678476-96678526	A549	lung:	n/a
40	chr2:96689067-96689117	HRE	kidney:	n/a
41	chr2:96689067-96689117	HIPEpiC	eye:	n/a
42	chr2:96679346-96679396	ProgFib	skin:	n/a
43	chr2:96689067-96689117	SAEC	small airway:	n/a
44	chr2:96678476-96678526	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:96679346-96679396	U87	brain:	n/a
46	chr2:96689067-96689117	K562	blood:	n/a
47	chr2:96689067-96689117	HEEpiC	esophagus:	n/a
48	chr2:96678476-96678526	MCF10A-Er-Src	breast:	n/a
49	chr2:96678476-96678526	AG04449	skin:	fetal
50	chr2:96679346-96679396	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96688619..96689595-chr2:97174117..97174910,2	K562	blood:
2	chr2:96687696..96690122-chr2:96838973..96841085,2	MCF-7	breast:
3	chr2:96678269..96680437-chr2:96873411..96875898,2	MCF-7	breast:
4	chr2:96678462..96681368-chr2:96930331..96932535,2	K562	blood:
5	chr2:96688443..96689089-chr2:96782413..96783451,3	MCF-7	breast:
6	chr2:96674813..96677740-chr2:96678852..96681143,2	K562	blood:
7	chr2:96688568..96689125-chr2:96840002..96840765,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIAO1-4	chr2:96679197-96679831	NONHSAT072533
2	lnc-CIAO1-4	chr2:96686873-96686981	NONHSAT072534
3	lnc-CIAO1-4	chr2:96687116-96687213	NONHSAT072534
4	lnc-GPAT2-2	chr2:96701600-96701713	NONHSAT072542
5	lnc-CIAO1-4	chr2:96688422-96688480	NONHSAT072534
6	lnc-CIAO1-4	chr2:96688422-96688882	NONHSAT072532
7	lnc-GPAT2-2	chr2:96700713-96700993	NONHSAT072542
8	lnc-CIAO1-4	chr2:96688854-96688882	NONHSAT072531

Variant related genes	Relation type
FAHD2CP	TF binding region
GPAT2	TF binding region
FAHD2CP	CpG island
GPAT2	CpG island
ENSG00000084090	chromatin interactions
ENSG00000231584	chromatin interactions
ENSG00000135956	chromatin interactions
ENSG00000144021	chromatin interactions
ENSG00000204685	chromatin interactions

Extended variants
information (count: 576 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569480145	chr2:96677857-96677858	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs148060300	chr2:96677861-96677862	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs550204703	chr2:96677957-96677958	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs543426809	chr2:96677982-96677983	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566923183	chr2:96678082-96678083	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs535799244	chr2:96678113-96678114	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs552659479	chr2:96678149-96678150	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566528595	chr2:96678172-96678173	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs549835669	chr2:96678189-96678190	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs79349986	chr2:96678207-96678208	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs2969476	chr2:96678214-96678215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs538480401	chr2:96678293-96678294	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577696486	chr2:96678375-96678376	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575483362	chr2:96678381-96678382	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544505878	chr2:96678412-96678413	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs555046161	chr2:96678549-96678550	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs574889628	chr2:96678550-96678551	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs540591132	chr2:96678565-96678566	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs560397299	chr2:96678632-96678633	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs547421330	chr2:96678692-96678693	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs532608713	chr2:96678819-96678820	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs529220394	chr2:96678832-96678833	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs546116041	chr2:96678965-96678966	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs563089578	chr2:96679084-96679085	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs531928653	chr2:96679088-96679089	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs548476189	chr2:96679113-96679114	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs547250545	chr2:96679148-96679149	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs568377047	chr2:96679163-96679164	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs189040930	chr2:96679165-96679166	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs376306212	chr2:96679166-96679167	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs529659105	chr2:96679241-96679242	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
32	rs377329740	chr2:96679242-96679243	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
33	rs566475454	chr2:96679256-96679257	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs538710266	chr2:96679263-96679264	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs552126091	chr2:96679304-96679305	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs569067855	chr2:96679336-96679337	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs144414917	chr2:96679340-96679341	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs2579517	chr2:96679384-96679385	Weak transcription Enhancers Strong transcription	CpG island Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs554912177	chr2:96679474-96679475	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
40	rs574749752	chr2:96679494-96679495	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs563309418	chr2:96679533-96679534	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs534205456	chr2:96679542-96679543	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs143867242	chr2:96679571-96679572	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs577308796	chr2:96679577-96679578	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
45	rs552660499	chr2:96679592-96679593	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
46	rs546275519	chr2:96679622-96679623	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
47	rs192660692	chr2:96679624-96679625	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
48	rs576241837	chr2:96679628-96679629	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
49	rs541987894	chr2:96679652-96679653	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
50	rs61740270	chr2:96679663-96679664	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96675600-96691400	Weak transcription	Gastric	stomach
2	chr2:96675800-96689000	Weak transcription	Spleen	Spleen
3	chr2:96676400-96679400	Weak transcription	Psoas Muscle	Psoas
4	chr2:96676400-96688400	Weak transcription	Colon Smooth Muscle	Colon
5	chr2:96677000-96678000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:96677000-96678200	Weak transcription	Left Ventricle	heart
7	chr2:96677000-96678400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:96677000-96678800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:96677000-96679000	Weak transcription	Fetal Stomach	stomach
10	chr2:96677000-96679400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:96677000-96680000	Weak transcription	Brain Germinal Matrix	brain
12	chr2:96677000-96681800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:96677000-96682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:96677000-96682800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:96677000-96685000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:96677000-96686200	Weak transcription	Pancreas	Pancrea
17	chr2:96677000-96688200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr2:96677000-96688200	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:96677000-96688400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:96677000-96690200	Weak transcription	Right Ventricle	heart
21	chr2:96677000-96690400	Weak transcription	Fetal Intestine Small	intestine
22	chr2:96677200-96678200	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr2:96677200-96678400	Weak transcription	Brain Anterior Caudate	brain
24	chr2:96677200-96680400	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr2:96677200-96680400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:96677200-96688200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr2:96677200-96688800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr2:96677400-96678000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:96677400-96678200	Weak transcription	Brain Hippocampus Middle	brain
30	chr2:96677400-96678400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr2:96677400-96684800	Weak transcription	Brain Angular Gyrus	brain
32	chr2:96677600-96678000	Weak transcription	Brain Substantia Nigra	brain
33	chr2:96677600-96678200	Enhancers	Brain Cingulate Gyrus	brain
34	chr2:96677600-96678600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr2:96677800-96678200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr2:96678000-96678800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:96678000-96679400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr2:96678000-96679800	Enhancers	Brain Substantia Nigra	brain
39	chr2:96678200-96678400	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr2:96678200-96678600	Flanking Active TSS	Brain Cingulate Gyrus	brain
41	chr2:96678200-96678600	Enhancers	Left Ventricle	heart
42	chr2:96678200-96678800	Enhancers	Brain Hippocampus Middle	brain
43	chr2:96678200-96678800	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr2:96678400-96678800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:96678400-96679400	Enhancers	Brain Anterior Caudate	brain
46	chr2:96678400-96679800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr2:96678600-96679600	Enhancers	Brain Cingulate Gyrus	brain
48	chr2:96678600-96691000	Weak transcription	Left Ventricle	heart
49	chr2:96678800-96681600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr2:96678800-96682800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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