Variant report

Variant	nsv605948
Chromosome Location	chr7:4137575-4167991
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	CBX3	chr7:4143342-4143771	K562	blood:	n/a	n/a
2	CEBPB	chr7:4143302-4143760	H1-hESC	embryonic stem cell:	n/a	chr7:4143746-4143757
3	CEBPB	chr7:4164261-4164462	A549	lung:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
4	CEBPB	chr7:4143145-4143844	MCF-7	breast:	n/a	chr7:4143746-4143757
5	CEBPB	chr7:4143335-4143889	K562	blood:	n/a	chr7:4143746-4143757
6	CEBPB	chr7:4143283-4143797	A549	lung:	n/a	chr7:4143746-4143757
7	CEBPB	chr7:4164281-4164504	HepG2	liver:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
8	CEBPB	chr7:4143725-4143868	HepG2	liver:	n/a	chr7:4143746-4143757
9	CHD2	chr7:4143451-4143520	K562	blood:	n/a	n/a
10	CTCF	chr7:4142020-4142170	HepG2	liver:	n/a	n/a
11	CTCF	chr7:4143134-4143457	Gliobla	brain:	n/a	chr7:4143161-4143179
12	CTCF	chr7:4143060-4143210	HPAF	blood vessel:	n/a	chr7:4143161-4143179
13	CTCF	chr7:4143078-4143280	HUVEC	blood vessel:	n/a	chr7:4143161-4143179
14	CTCF	chr7:4146220-4146370	HRE	kidney:	n/a	n/a
15	CTCF	chr7:4143160-4143310	HRE	kidney:	n/a	chr7:4143161-4143179
16	CTCF	chr7:4143113-4143226	LNCaP	prostate:	n/a	chr7:4143161-4143179
17	CTCF	chr7:4143021-4143331	HepG2	liver:	n/a	chr7:4143161-4143179
18	CTCF	chr7:4143120-4143270	HRPEpiC	eye:	n/a	chr7:4143161-4143179
19	CTCF	chr7:4142940-4143090	HEK293	kidney:	n/a	n/a
20	CTCF	chr7:4143100-4143250	RPTEC	kidney:	n/a	chr7:4143161-4143179
21	CTCF	chr7:4143019-4143302	K562	blood:	n/a	chr7:4143161-4143179
22	CTCF	chr7:4143060-4143210	HMF	breast:	n/a	chr7:4143161-4143179
23	CTCF	chr7:4142840-4142990	HCT-116	colon:	n/a	n/a
24	CTCF	chr7:4143160-4143310	MCF-7	breast:	n/a	chr7:4143161-4143179
25	CTCF	chr7:4143100-4143250	Hela-S3	cervix:	n/a	chr7:4143161-4143179
26	CTCF	chr7:4143079-4143270	LNCaP	prostate:	n/a	chr7:4143161-4143179
27	CTCF	chr7:4143120-4143270	HCT-116	colon:	n/a	chr7:4143161-4143179
28	CTCF	chr7:4143060-4143210	HPF	lung:	n/a	chr7:4143161-4143179
29	CTCF	chr7:4142920-4143070	A549	lung:	n/a	n/a
30	CTCF	chr7:4143020-4143170	GM12867	blood:	n/a	n/a
31	CTCF	chr7:4143353-4143425	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:4143092-4143243	HepG2	liver:	n/a	chr7:4143161-4143179
33	CTCF	chr7:4143122-4143251	MCF-7	breast:	n/a	chr7:4143161-4143179
34	CTCF	chr7:4143040-4143190	SK-N-SH_RA	brain:	n/a	chr7:4143161-4143179
35	CTCF	chr7:4143120-4143270	HUVEC	blood vessel:	n/a	chr7:4143161-4143179
36	CTCF	chr7:4143040-4143190	Caco-2	colon:	n/a	chr7:4143161-4143179
37	CTCF	chr7:4142480-4142630	HAc	cerebellar:	n/a	n/a
38	CTCF	chr7:4143109-4143186	Spleen_OC	spleen:	n/a	chr7:4143161-4143179
39	CTCF	chr7:4143400-4143550	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr7:4143060-4143210	NHEK	skin:	n/a	chr7:4143161-4143179
41	CTCF	chr7:4143060-4143210	HCFaa	heart:	n/a	chr7:4143161-4143179
42	CTCF	chr7:4143120-4143270	NB4	blood:	n/a	chr7:4143161-4143179
43	CTCF	chr7:4142960-4143110	HepG2	liver:	n/a	n/a
44	CTCF	chr7:4143380-4143530	HPF	lung:	n/a	n/a
45	CTCF	chr7:4143090-4143389	MCF-7	breast:	n/a	chr7:4143161-4143179
46	CTCF	chr7:4143140-4143290	MCF-7	breast:	n/a	chr7:4143161-4143179
47	CTCF	chr7:4143061-4143307	H1-hESC	embryonic stem cell:	n/a	chr7:4143161-4143179
48	CTCF	chr7:4143120-4143270	Hela-S3	cervix:	n/a	chr7:4143161-4143179
49	CTCF	chr7:4142940-4143090	HRE	kidney:	n/a	n/a
50	CTCF	chr7:4143320-4143470	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4153707-4153757	IMR90	lung:	fetal
2	chr7:4153707-4153757	IMR90	lung:	fetal
3	chr7:4153732-4153782	A549	lung:	n/a
4	chr7:4153767-4153817	AG10803	skin:	n/a
5	chr7:4153707-4153757	HUVEC	blood vessel:	n/a
6	chr7:4146971-4147021	BJ	skin:	n/a
7	chr7:4153707-4153757	HCPEpiC	choroid plexus:	n/a
8	chr7:4150753-4150803	PANC-1	pancreas:	n/a
9	chr7:4167607-4167657	ProgFib	skin:	n/a
10	chr7:4146971-4147021	LNCaP	prostate:	n/a
11	chr7:4152976-4153026	AG04450	lung:	fetal
12	chr7:4167882-4167932	Hela-S3	cervix:	n/a
13	chr7:4153868-4153918	HUVEC	blood vessel:	n/a
14	chr7:4167809-4167859	Hepatocyte	liver:	n/a
15	chr7:4153919-4153969	AG09319	gingival:	n/a
16	chr7:4147330-4147380	AG04449	skin:	fetal
17	chr7:4167943-4167993	Jurkat	blood:	n/a
18	chr7:4157691-4157741	Hepatocyte	liver:	n/a
19	chr7:4147330-4147380	HIPEpiC	eye:	n/a
20	chr7:4167809-4167859	ProgFib	skin:	n/a
21	chr7:4153767-4153817	HAEpiC	amniotic membrane:	n/a
22	chr7:4167607-4167657	IMR90	lung:	fetal
23	chr7:4153732-4153782	HCT-116	colon:	n/a
24	chr7:4152953-4153003	Hepatocyte	liver:	n/a
25	chr7:4147432-4147482	SAEC	small airway:	n/a
26	chr7:4152976-4153026	MCF-7	breast:	n/a
27	chr7:4167882-4167932	GM12891	blood:	n/a
28	chr7:4167411-4167461	Hela-S3	cervix:	n/a
29	chr7:4147432-4147482	T-47D	breast:	n/a
30	chr7:4152976-4153026	PANC-1	pancreas:	n/a
31	chr7:4153767-4153817	HRPEpiC	eye:	n/a
32	chr7:4153767-4153817	NHDF-neo	bronchial:	n/a
33	chr7:4153732-4153782	ovcar-3	ovarian:	n/a
34	chr7:4167411-4167461	NT2-D1	testis:	n/a
35	chr7:4147432-4147482	HEEpiC	esophagus:	n/a
36	chr7:4147432-4147482	GM12891	blood:	n/a
37	chr7:4153707-4153757	HCM	heart:	n/a
38	chr7:4167943-4167993	ProgFib	skin:	n/a
39	chr7:4147274-4147324	RPTEC	kidney:	n/a
40	chr7:4153707-4153757	Caco-2	colon:	n/a
41	chr7:4147432-4147482	BJ	skin:	n/a
42	chr7:4147432-4147482	BE2_C	brain:	n/a
43	chr7:4167943-4167993	SK-N-SH	brain:	n/a
44	chr7:4147330-4147380	HEK293	kidney:	embryo
45	chr7:4153767-4153817	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:4167943-4167993	HEEpiC	esophagus:	n/a
47	chr7:4147274-4147324	NT2-D1	testis:	n/a
48	chr7:4157691-4157741	AG04450	lung:	fetal
49	chr7:4167943-4167993	BJ	skin:	n/a
50	chr7:4146291-4146341	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:
2	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:
3	chr7:4130773..4135650-chr7:4142053..4144303,4	MCF-7	breast:
4	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
5	chr7:4133522..4135936-chr7:4136765..4138658,2	K562	blood:
6	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
7	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island

Extended variants
information (count: 1761 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1761 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13223093	chr7:4137575-4137576	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113927191	chr7:4137578-4137579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150318597	chr7:4137591-4137592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560918929	chr7:4137619-4137620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551746445	chr7:4137635-4137636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139200930	chr7:4137648-4137649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144019209	chr7:4137687-4137688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569689728	chr7:4137702-4137703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563536944	chr7:4137842-4137843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532202429	chr7:4137871-4137872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552309823	chr7:4137900-4137901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10270432	chr7:4137922-4137923	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs528370222	chr7:4137923-4137924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146435763	chr7:4137939-4137940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115117116	chr7:4137940-4137941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537185400	chr7:4137952-4137953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181214685	chr7:4137956-4137957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185041339	chr7:4137982-4137983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538867486	chr7:4137983-4137984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139810220	chr7:4138025-4138026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75610162	chr7:4138036-4138037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573319608	chr7:4138038-4138039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534961642	chr7:4138070-4138071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554574676	chr7:4138112-4138113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188561174	chr7:4138121-4138122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112067082	chr7:4138122-4138123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549096506	chr7:4138129-4138130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10240423	chr7:4138138-4138139	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs577236223	chr7:4138142-4138143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545704390	chr7:4138146-4138147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559479783	chr7:4138188-4138189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575608104	chr7:4138197-4138198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548494203	chr7:4138225-4138226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180706544	chr7:4138236-4138237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530524758	chr7:4138257-4138258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559339108	chr7:4138300-4138301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373273513	chr7:4138310-4138311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142234863	chr7:4138360-4138361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537890228	chr7:4138367-4138368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185140322	chr7:4138369-4138370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570467813	chr7:4138406-4138407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539490018	chr7:4138411-4138412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552521414	chr7:4138421-4138422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77266499	chr7:4138456-4138457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs398047570	chr7:4138457-4138458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs58678214	chr7:4138483-4138484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539869143	chr7:4138484-4138485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35261674	chr7:4138491-4138492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558170501	chr7:4138495-4138496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573122892	chr7:4138496-4138497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4119400-4153000	Weak transcription	Gastric	stomach
2	chr7:4129400-4150000	Weak transcription	Pancreas	Pancrea
3	chr7:4131800-4143400	Weak transcription	Fetal Intestine Small	intestine
4	chr7:4132200-4141600	Weak transcription	Fetal Stomach	stomach
5	chr7:4132400-4180200	Weak transcription	Colon Smooth Muscle	Colon
6	chr7:4134400-4139200	Weak transcription	Spleen	Spleen
7	chr7:4135800-4138200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr7:4136400-4137600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr7:4136600-4137600	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr7:4136600-4139200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:4136600-4139400	Enhancers	Primary T cells from cord blood	blood
12	chr7:4136800-4140000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:4136800-4141200	Weak transcription	Lung	lung
14	chr7:4137000-4137600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr7:4137000-4137600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr7:4137000-4138200	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr7:4137200-4141400	Weak transcription	Fetal Muscle Leg	muscle
18	chr7:4137200-4149400	Weak transcription	Aorta	Aorta
19	chr7:4137600-4139400	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr7:4139200-4139400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:4139200-4139400	Enhancers	Spleen	Spleen
22	chr7:4139400-4139800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr7:4139400-4139800	Weak transcription	Spleen	Spleen
24	chr7:4139600-4139800	Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr7:4139800-4142000	Enhancers	Spleen	Spleen
26	chr7:4139800-4142200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr7:4139800-4143200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:4140000-4140800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:4140000-4141200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:4140800-4149000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:4141200-4141400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr7:4141200-4141400	Enhancers	Lung	lung
33	chr7:4141200-4142400	Enhancers	Fetal Muscle Trunk	muscle
34	chr7:4141400-4141800	Enhancers	Fetal Muscle Leg	muscle
35	chr7:4141400-4142000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:4141400-4142000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:4141400-4142000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr7:4141400-4142200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:4141400-4142200	Enhancers	Fetal Lung	lung
40	chr7:4141400-4142400	Enhancers	Fetal Brain Male	brain
41	chr7:4141400-4142400	Enhancers	Fetal Brain Female	brain
42	chr7:4141400-4144000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr7:4141600-4142000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr7:4141600-4142200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:4141600-4142200	Enhancers	Fetal Stomach	stomach
46	chr7:4141600-4142400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:4141800-4142200	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr7:4142000-4145400	Weak transcription	Spleen	Spleen
49	chr7:4142000-4150200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:4142200-4142400	Enhancers	Skeletal Muscle Male	skeletal muscle

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