Variant report

Variant	esv1796312
Chromosome Location	chr4:560701-569738
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	BACH1	chr4:569194-569394	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:563800-564052	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr4:569385-569452	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr4:565828-565840	HepG2	liver:	n/a	n/a
5	CTCF	chr4:569120-569270	HCPEpiC	choroid plexus:	n/a	chr4:569137-569150
6	CTCF	chr4:569154-569260	NHEK	skin:	n/a	n/a
7	E2F6	chr4:568697-569379	H1-hESC	embryonic stem cell:	n/a	chr4:568834-568843
8	EP300	chr4:563141-563198	GM12878	blood:	n/a	n/a
9	ESR1	chr4:563828-564129	T-47D	breast:	n/a	chr4:564056-564073 chr4:564031-564046 chr4:564031-564048 chr4:564057-564072
10	ESR1	chr4:563895-564120	T-47D	breast:	n/a	chr4:564056-564073 chr4:564031-564046 chr4:564031-564048 chr4:564057-564072
11	JUND	chr4:565363-565399	H1-hESC	embryonic stem cell:	n/a	n/a
12	KAP1	chr4:565856-566180	HEK293	kidney:	n/a	n/a
13	MAFF	chr4:564692-564911	HepG2	liver:	n/a	chr4:564800-564818
14	MAFK	chr4:564736-564853	HepG2	liver:	n/a	chr4:564804-564818 chr4:564801-564816 chr4:564806-564817 chr4:564806-564817 chr4:564805-564816 chr4:564805-564816
15	MAFK	chr4:564729-564928	HepG2	liver:	n/a	chr4:564804-564818 chr4:564801-564816 chr4:564806-564817 chr4:564806-564817 chr4:564805-564816 chr4:564805-564816
16	MAX	chr4:569042-569452	ECC-1	luminal epithelium:	n/a	n/a
17	MAX	chr4:564134-564543	NB4	blood:	n/a	chr4:564362-564372 chr4:564378-564388
18	MAX	chr4:564197-564413	K562	blood:	n/a	chr4:564362-564372 chr4:564378-564388
19	MAX	chr4:569027-569418	ECC-1	luminal epithelium:	n/a	n/a
20	MAX	chr4:564072-564482	K562	blood:	n/a	chr4:564362-564372 chr4:564378-564388
21	MAX	chr4:568444-568978	H1-hESC	embryonic stem cell:	n/a	chr4:568550-568560 chr4:568884-568891 chr4:568549-568557
22	MAX	chr4:568478-569455	H1-hESC	embryonic stem cell:	n/a	chr4:568550-568560 chr4:568884-568891 chr4:568549-568557
23	MAX	chr4:569031-569384	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAX	chr4:569061-569321	SK-N-SH	brain:	n/a	n/a
25	MAX	chr4:564066-564401	K562	blood:	n/a	chr4:564362-564372 chr4:564378-564388
26	MAZ	chr4:569071-569497	IMR90	lung:	n/a	n/a
27	MXI1	chr4:569095-569346	H1-hESC	embryonic stem cell:	n/a	n/a
28	MXI1	chr4:569053-569451	IMR90	lung:	n/a	n/a
29	MYC	chr4:568483-568592	H1-hESC	embryonic stem cell:	n/a	chr4:568550-568560 chr4:568549-568557
30	MYC	chr4:565906-565917	MCF-7	breast:	n/a	n/a
31	MYC	chr4:564192-564281	MCF-7	breast:	n/a	n/a
32	MYC	chr4:564092-564106	MCF-7	breast:	n/a	n/a
33	MYC	chr4:565807-565823	MCF-7	breast:	n/a	n/a
34	MYC	chr4:566069-566087	MCF-7	breast:	n/a	n/a
35	MYC	chr4:565831-565900	MCF-7	breast:	n/a	n/a
36	MYC	chr4:566088-566182	HUVEC	blood vessel:	n/a	n/a
37	MYC	chr4:565892-565900	MCF-7	breast:	n/a	n/a
38	MYC	chr4:565871-565873	MCF-7	breast:	n/a	n/a
39	MYC	chr4:566125-566153	MCF-7	breast:	n/a	n/a
40	MYC	chr4:566087-566153	MCF-7	breast:	n/a	n/a
41	MYC	chr4:565946-566110	MCF-7	breast:	n/a	n/a
42	POLR2A	chr4:565975-565979	A549	lung:	n/a	n/a
43	POLR2A	chr4:565785-566229	MCF-7	breast:	n/a	n/a
44	POLR2A	chr4:566001-566153	MCF-7	breast:	n/a	n/a
45	POLR2A	chr4:565833-566329	H1-neurons	neurons:	n/a	n/a
46	POLR2A	chr4:565622-566213	SK-N-MC	brain:	n/a	n/a
47	POLR2A	chr4:569033-571774	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr4:565981-566217	A549	lung:	n/a	n/a
49	POLR2A	chr4:569134-569306	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr4:568722-570035	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:565955-566005	HRCEpiC	kidney:	n/a
2	chr4:568298-568348	ProgFib	skin:	n/a
3	chr4:565955-566005	HRCEpiC	kidney:	n/a
4	chr4:568298-568348	ProgFib	skin:	n/a
5	chr4:568205-568255	HRPEpiC	eye:	n/a
6	chr4:565955-566005	PrEC	prostate:	n/a
7	chr4:568514-568564	T-47D	breast:	n/a
8	chr4:568298-568348	HIPEpiC	eye:	n/a
9	chr4:568205-568255	SAEC	small airway:	n/a
10	chr4:568514-568564	H1-hESC	embryonic stem cell:	embryo
11	chr4:567537-567587	HUVEC	blood vessel:	n/a
12	chr4:568205-568255	Caco-2	colon:	n/a
13	chr4:565955-566005	HAEpiC	amniotic membrane:	n/a
14	chr4:568298-568348	K562	blood:	n/a
15	chr4:568205-568255	MCF10A-Er-Src	breast:	n/a
16	chr4:568514-568564	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:568298-568348	MCF-7	breast:	n/a
18	chr4:565955-566005	GM06990	blood:	n/a
19	chr4:568205-568255	SK-N-SH	brain:	n/a
20	chr4:567537-567587	AG10803	skin:	n/a
21	chr4:568298-568348	HAEpiC	amniotic membrane:	n/a
22	chr4:569174-569224	GM06990	blood:	n/a
23	chr4:567537-567587	HEK293	kidney:	embryo
24	chr4:567537-567587	H1-hESC	embryonic stem cell:	embryo
25	chr4:568298-568348	H1-hESC	embryonic stem cell:	embryo
26	chr4:569174-569224	SKMC	muscle:	n/a
27	chr4:567537-567587	NHDF-neo	bronchial:	n/a
28	chr4:568514-568564	MCF10A-Er-Src	breast:	n/a
29	chr4:569174-569224	GM12878	blood:	n/a
30	chr4:568205-568255	ProgFib	skin:	n/a
31	chr4:568298-568348	RPTEC	kidney:	n/a
32	chr4:568298-568348	PANC-1	pancreas:	n/a
33	chr4:568298-568348	HMEC	breast:	n/a
34	chr4:568205-568255	HCT-116	colon:	n/a
35	chr4:565955-566005	SK-N-MC	brain:	n/a
36	chr4:568205-568255	CMK	blood:	n/a
37	chr4:565955-566005	K562	blood:	n/a
38	chr4:568514-568564	BJ	skin:	n/a
39	chr4:568205-568255	NHDF-neo	bronchial:	n/a
40	chr4:565955-566005	ProgFib	skin:	n/a
41	chr4:568514-568564	BE2_C	brain:	n/a
42	chr4:569174-569224	NB4	blood:	n/a
43	chr4:569174-569224	NT2-D1	testis:	n/a
44	chr4:567537-567587	HMEC	breast:	n/a
45	chr4:568205-568255	SK-N-SH_RA	brain:	n/a
46	chr4:567537-567587	AG04449	skin:	fetal
47	chr4:565955-566005	PFSK-1	brain:	n/a
48	chr4:569174-569224	HCT-116	colon:	n/a
49	chr4:568205-568255	NT2-D1	testis:	n/a
50	chr4:568514-568564	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:560309..561984-chr4:571273..573145,2	K562	blood:
2	chr4:560447..562765-chr4:571972..574666,2	MCF-7	breast:
3	chr4:565489..567950-chr4:568759..571284,3	MCF-7	breast:
4	chr4:564165..566404-chr4:569838..571549,2	K562	blood:
5	chr4:560744..563501-chr4:564361..568313,3	K562	blood:
6	chr4:564200..566117-chr4:572319..574456,3	K562	blood:
7	chr4:565489..567950-chr4:568759..571284,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGG-1	chr4:562509-568807	l_2577_chr4:560751-568807_brain
2	lnc-PIGG-1	chr4:560752-561223	l_2577_chr4:560751-568807_brain
3	lnc-ZNF721-4	chr4:567669-568201	ENSG00000273238.1

Variant related genes	Relation type
ENSG00000273238	TF binding region
ENSG00000273238	CpG island
ENSG00000273238	chromatin interactions

Extended variants
information (count: 357 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576822966	chr4:560749-560750	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs189190394	chr4:560797-560798	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs182387274	chr4:560829-560830	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs142349888	chr4:560830-560831	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs114503376	chr4:560842-560843	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs73074224	chr4:560897-560898	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs527524852	chr4:560903-560904	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs78233832	chr4:560926-560927	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs564422059	chr4:560936-560937	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs531287709	chr4:560947-560948	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs549814352	chr4:561061-561062	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs568030644	chr4:561068-561069	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs73219270	chr4:561121-561122	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187385673	chr4:561220-561221	ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs536606083	chr4:561221-561222	ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs146161359	chr4:561307-561308	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534169388	chr4:561312-561313	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375564293	chr4:561418-561419	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558778886	chr4:561443-561444	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs386670404	chr4:561466-561467	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114710984	chr4:561468-561469	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370129749	chr4:561495-561496	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537812484	chr4:561496-561497	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556541580	chr4:561504-561505	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190447158	chr4:561505-561506	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116960925	chr4:561529-561530	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs79091673	chr4:561551-561552	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368688454	chr4:561577-561578	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572205014	chr4:561591-561592	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576428011	chr4:561594-561595	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546025917	chr4:561606-561607	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564333681	chr4:561615-561616	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12639825	chr4:561628-561629	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7655590	chr4:561631-561632	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs141530096	chr4:561691-561692	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs78711764	chr4:561705-561706	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547873645	chr4:561708-561709	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150870257	chr4:561726-561727	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547465117	chr4:561891-561892	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs372723940	chr4:561968-561969	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139306901	chr4:561988-561989	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368432603	chr4:561995-561996	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552368052	chr4:562028-562029	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs35839284	chr4:562043-562044	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558986375	chr4:562102-562103	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538125844	chr4:562139-562140	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534775476	chr4:562154-562155	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181638852	chr4:562158-562159	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535528970	chr4:562191-562192	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs33972056	chr4:562200-562201	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:561200-561800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:561600-562200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:561800-562200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:562200-563800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:563800-564000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:563800-564400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:563800-564400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:564000-564400	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:564200-564400	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:564200-564400	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr4:564400-564800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:564400-565800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:564600-564800	Bivalent Enhancer	Placenta	Placenta
14	chr4:565600-565800	Bivalent Enhancer	Fetal Brain Female	brain
15	chr4:565600-567200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr4:565800-566200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:565800-566200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:565800-566200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
19	chr4:565800-566200	ZNF genes & repeats	Gastric	stomach
20	chr4:565800-567000	Enhancers	Brain Angular Gyrus	brain
21	chr4:565800-567800	Bivalent Enhancer	Fetal Brain Male	brain
22	chr4:566000-566200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:566200-568600	Weak transcription	Gastric	stomach
24	chr4:566600-567200	Bivalent Enhancer	Fetal Brain Female	brain
25	chr4:566800-567000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
26	chr4:567000-567400	Bivalent Enhancer	Brain Anterior Caudate	brain
27	chr4:567000-567400	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
28	chr4:567200-567400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:567200-567600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
30	chr4:567200-572200	Active TSS	Brain Angular Gyrus	brain
31	chr4:567400-567600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:567400-567600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
33	chr4:567400-567600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
34	chr4:567400-567600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr4:567400-568800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr4:567400-569000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
37	chr4:567600-567800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
38	chr4:567600-567800	Bivalent Enhancer	Fetal Brain Female	brain
39	chr4:567600-568200	Weak transcription	Spleen	Spleen
40	chr4:567600-570800	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr4:567800-568200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
42	chr4:567800-568200	Bivalent/Poised TSS	Fetal Brain Female	brain
43	chr4:568000-568400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
44	chr4:568200-568400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
45	chr4:568200-568400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr4:568200-568400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:568200-568400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
48	chr4:568200-568400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
49	chr4:568200-568400	Bivalent Enhancer	Fetal Intestine Small	intestine
50	chr4:568200-568600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell

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