Variant report

Variant	esv3359334
Chromosome Location	chr4:684502-687300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:79)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:79 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:687028-687335	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:687024-687244	K562	blood:	n/a	n/a
3	BHLHE40	chr4:686937-687418	HepG2	liver:	n/a	n/a
4	CCNT2	chr4:686870-686943	K562	blood:	n/a	n/a
5	CEBPB	chr4:685791-685837	K562	blood:	n/a	n/a
6	CEBPD	chr4:687062-687371	HepG2	liver:	n/a	n/a
7	CHD2	chr4:687103-687248	HepG2	liver:	n/a	n/a
8	E2F6	chr4:686521-686730	K562	blood:	n/a	n/a
9	ELF1	chr4:686626-687357	MCF-7	breast:	n/a	n/a
10	ELF1	chr4:686538-687130	MCF-7	breast:	n/a	n/a
11	EP300	chr4:687068-687271	HepG2	liver:	n/a	n/a
12	EP300	chr4:686919-687397	HepG2	liver:	n/a	n/a
13	FOSL2	chr4:687044-687383	HepG2	liver:	n/a	n/a
14	FOXA1	chr4:685311-685508	T-47D	breast:	n/a	n/a
15	FOXA1	chr4:686884-687371	HepG2	liver:	n/a	n/a
16	FOXA1	chr4:686950-687520	HepG2	liver:	n/a	n/a
17	FOXA1	chr4:686777-687371	T-47D	breast:	n/a	n/a
18	FOXA1	chr4:686914-687356	T-47D	breast:	n/a	n/a
19	FOXA1	chr4:686923-687387	HepG2	liver:	n/a	n/a
20	FOXA1	chr4:686940-687498	HepG2	liver:	n/a	n/a
21	FOXA2	chr4:687033-687335	A549	lung:	n/a	n/a
22	FOXA2	chr4:686670-687631	HepG2	liver:	n/a	n/a
23	FOXA2	chr4:686929-687299	A549	lung:	n/a	n/a
24	FOXA2	chr4:687045-687362	HepG2	liver:	n/a	n/a
25	GATA3	chr4:686451-687256	MCF-7	breast:	n/a	chr4:686690-686700 chr4:686692-686709 chr4:686880-686890 chr4:686691-686700
26	GATA3	chr4:686369-687104	MCF-7	breast:	n/a	chr4:686690-686700 chr4:686692-686709 chr4:686880-686890 chr4:686691-686700
27	GATA3	chr4:686669-687138	MCF-7	breast:	n/a	chr4:686690-686700 chr4:686692-686709 chr4:686880-686890 chr4:686691-686700
28	GATA3	chr4:686373-686776	T-47D	breast:	n/a	chr4:686690-686700 chr4:686692-686709 chr4:686691-686700
29	GATA3	chr4:686314-686945	T-47D	breast:	n/a	chr4:686690-686700 chr4:686692-686709 chr4:686880-686890 chr4:686691-686700
30	HDAC2	chr4:686598-687362	MCF-7	breast:	n/a	chr4:686696-686715
31	HMGN3	chr4:686837-686967	K562	blood:	n/a	n/a
32	MAFF	chr4:684519-684741	HepG2	liver:	n/a	chr4:684607-684625
33	MAFF	chr4:687046-687145	HepG2	liver:	n/a	n/a
34	MAFK	chr4:684555-684755	HepG2	liver:	n/a	n/a
35	MAX	chr4:686528-687359	MCF-7	breast:	n/a	n/a
36	MAX	chr4:687010-687339	HepG2	liver:	n/a	n/a
37	MAX	chr4:686545-687415	MCF-7	breast:	n/a	n/a
38	MAX	chr4:686711-687442	HepG2	liver:	n/a	n/a
39	MAX	chr4:686750-687483	HepG2	liver:	n/a	n/a
40	MAX	chr4:686438-687343	K562	blood:	n/a	n/a
41	MAZ	chr4:687099-687327	HepG2	liver:	n/a	n/a
42	MAZ	chr4:686591-686741	K562	blood:	n/a	n/a
43	MBD4	chr4:687002-687311	HepG2	liver:	n/a	n/a
44	MXI1	chr4:686953-687405	HepG2	liver:	n/a	n/a
45	MYBL2	chr4:687044-687325	HepG2	liver:	n/a	n/a
46	MYBL2	chr4:686870-687426	HepG2	liver:	n/a	n/a
47	MYC	chr4:686626-687351	MCF-7	breast:	n/a	n/a
48	MYC	chr4:686918-686980	MCF-7	breast:	n/a	n/a
49	MYC	chr4:686907-686916	MCF-7	breast:	n/a	n/a
50	MYC	chr4:687031-687050	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:687023-687073	ovcar-3	ovarian:	n/a
2	chr4:686870-686920	HL-60	blood:	n/a
3	chr4:687023-687073	HUVEC	blood vessel:	n/a
4	chr4:686870-686920	SK-N-SH	brain:	n/a
5	chr4:686870-686920	MCF-7	breast:	n/a
6	chr4:686870-686920	Hepatocyte	liver:	n/a
7	chr4:687023-687073	SKMC	muscle:	n/a
8	chr4:686870-686920	HCT-116	colon:	n/a
9	chr4:686870-686920	HRPEpiC	eye:	n/a
10	chr4:687023-687073	A549	lung:	n/a
11	chr4:687023-687073	U87	brain:	n/a
12	chr4:687023-687073	AG09319	gingival:	n/a
13	chr4:687023-687073	NT2-D1	testis:	n/a
14	chr4:686870-686920	GM12892	blood:	n/a
15	chr4:687023-687073	SAEC	small airway:	n/a
16	chr4:687023-687073	AoSMC	blood vessel:	n/a
17	chr4:687023-687073	GM12892	blood:	n/a
18	chr4:687023-687073	AG04449	skin:	fetal
19	chr4:687023-687073	HL-60	blood:	n/a
20	chr4:686870-686920	A549	lung:	n/a
21	chr4:687023-687073	HepG2	liver:	n/a
22	chr4:687023-687073	HIPEpiC	eye:	n/a
23	chr4:686870-686920	AG09319	gingival:	n/a
24	chr4:687023-687073	HMEC	breast:	n/a
25	chr4:687023-687073	HRPEpiC	eye:	n/a
26	chr4:687023-687073	AG04450	lung:	fetal
27	chr4:687023-687073	CMK	blood:	n/a
28	chr4:687023-687073	RPTEC	kidney:	n/a
29	chr4:687023-687073	NB4	blood:	n/a
30	chr4:686870-686920	HRCEpiC	kidney:	n/a
31	chr4:686870-686920	SK-N-SH_RA	brain:	n/a
32	chr4:686870-686920	HIPEpiC	eye:	n/a
33	chr4:686870-686920	NHDF-neo	bronchial:	n/a
34	chr4:687023-687073	BE2_C	brain:	n/a
35	chr4:686870-686920	ECC-1	luminal epithelium:	n/a
36	chr4:686870-686920	Jurkat	blood:	n/a
37	chr4:686870-686920	IMR90	lung:	fetal
38	chr4:686870-686920	ovcar-3	ovarian:	n/a
39	chr4:687023-687073	NH-A	brain:	n/a
40	chr4:687023-687073	NHDF-neo	bronchial:	n/a
41	chr4:686870-686920	SK-N-MC	brain:	n/a
42	chr4:686870-686920	GM06990	blood:	n/a
43	chr4:686870-686920	PANC-1	pancreas:	n/a
44	chr4:687023-687073	Caco-2	colon:	n/a
45	chr4:687023-687073	GM06990	blood:	n/a
46	chr4:687023-687073	HEEpiC	esophagus:	n/a
47	chr4:686870-686920	SAEC	small airway:	n/a
48	chr4:686870-686920	HCPEpiC	choroid plexus:	n/a
49	chr4:687023-687073	T-47D	breast:	n/a
50	chr4:687023-687073	SK-N-SH	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:665734..668691-chr4:686720..689048,2	K562	blood:
2	chr4:685366..688293-chr4:699391..702388,2	K562	blood:
3	chr4:685168..687948-chr4:720872..722966,2	K562	blood:
4	chr4:684734..689107-chr4:696185..700611,4	MCF-7	breast:
5	chr4:675712..677367-chr4:684331..686436,2	MCF-7	breast:
6	chr4:681142..683138-chr4:683907..688353,5	MCF-7	breast:
7	chr4:648535..651226-chr4:685340..688020,2	MCF-7	breast:
8	chr4:684700..687240-chr4:700658..702428,2	MCF-7	breast:
9	chr4:672624..674794-chr4:684663..687063,2	MCF-7	breast:
10	chr4:687290..688821-chr4:702192..704645,2	MCF-7	breast:
11	chr4:686727..688524-chr4:699007..701033,3	K562	blood:
12	chr4:670559..672271-chr4:686470..688637,2	MCF-7	breast:

No data

Variant related genes	Relation type
MFSD7	TF binding region
MFSD7	CpG island
ENSG00000185619	chromatin interactions
ENSG00000215375	chromatin interactions
ENSG00000242686	chromatin interactions
ENSG00000169026	chromatin interactions
ENSG00000169020	chromatin interactions

Extended variants
information (count: 135 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:135 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376185879	chr4:684511-684512	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375288230	chr4:684526-684527	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561189381	chr4:684591-684592	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528057280	chr4:684610-684611	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546646388	chr4:684613-684614	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571361018	chr4:684618-684619	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs139281994	chr4:684654-684655	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550658404	chr4:684751-684752	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs570100843	chr4:684800-684801	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs149565483	chr4:684803-684804	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs555602779	chr4:684823-684824	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs574026167	chr4:684825-684826	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs185835813	chr4:684917-684918	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs552998752	chr4:685011-685012	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs371541364	chr4:685071-685072	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs397992094	chr4:685089-685090	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs577708773	chr4:685109-685110	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs545133314	chr4:685134-685135	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs557431921	chr4:685158-685159	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs147256841	chr4:685172-685173	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs542823989	chr4:685210-685211	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs140713128	chr4:685218-685219	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs145313245	chr4:685331-685332	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs546471147	chr4:685370-685371	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs573480980	chr4:685376-685377	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs577188870	chr4:685383-685384	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs71166827	chr4:685393-685394	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs535647470	chr4:685397-685398	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs541130272	chr4:685407-685408	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs553636423	chr4:685409-685410	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs564827278	chr4:685410-685411	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs74847579	chr4:685418-685419	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs188854269	chr4:685422-685423	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs181442159	chr4:685430-685431	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs184393544	chr4:685522-685523	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs530993899	chr4:685527-685528	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs559781401	chr4:685537-685538	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs188391742	chr4:685538-685539	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs111397494	chr4:685541-685542	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs79407845	chr4:685547-685548	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs567619296	chr4:685551-685552	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs562074262	chr4:685562-685563	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs535027996	chr4:685605-685606	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs559864032	chr4:685657-685658	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs12500303	chr4:685660-685661	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs539046780	chr4:685666-685667	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs181588642	chr4:685748-685749	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs11248032	chr4:685756-685757	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs142150189	chr4:685779-685780	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs78121920	chr4:685801-685802	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:682200-686400	Weak transcription	K562	blood
2	chr4:683000-684600	Enhancers	Spleen	Spleen
3	chr4:683200-684600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr4:683200-685000	Weak transcription	Ovary	ovary
5	chr4:683400-684600	Enhancers	Pancreas	Pancrea
6	chr4:683600-684600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:683600-686400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr4:683600-686600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr4:683600-686600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr4:683600-686800	Weak transcription	Liver	Liver
11	chr4:683600-697200	Weak transcription	Gastric	stomach
12	chr4:683600-699000	Weak transcription	Right Atrium	heart
13	chr4:683800-684600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:683800-684600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr4:683800-684600	Enhancers	Duodenum Mucosa	Duodenum
16	chr4:683800-686400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:683800-686400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr4:683800-686600	Weak transcription	Fetal Thymus	thymus
19	chr4:683800-687600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr4:683800-689000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr4:684000-685200	Weak transcription	Placenta	Placenta
22	chr4:684000-686400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr4:684000-686400	Weak transcription	Fetal Lung	lung
24	chr4:684200-689800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr4:684200-699000	Weak transcription	Right Ventricle	heart
26	chr4:684400-684600	Bivalent Enhancer	HepG2	liver
27	chr4:684400-686600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr4:684400-686800	Weak transcription	Esophagus	oesophagus
29	chr4:684400-687200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr4:684400-687600	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr4:684400-693400	Weak transcription	Fetal Intestine Small	intestine
32	chr4:684600-686000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:685200-688600	Enhancers	Placenta	Placenta
34	chr4:685800-687800	Bivalent Enhancer	HepG2	liver
35	chr4:686000-686200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:686200-686600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:686400-686600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr4:686400-686600	Enhancers	Fetal Lung	lung
39	chr4:686400-687200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:686400-687200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr4:686400-687200	Enhancers	Placenta Amnion	Placenta Amnion
42	chr4:686400-687200	Enhancers	K562	blood
43	chr4:686400-688000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:686600-686800	Enhancers	Fetal Thymus	thymus
45	chr4:686600-686800	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr4:686600-687000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr4:686600-687000	Enhancers	H1 Cell Line	embryonic stem cell
48	chr4:686600-687000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:686600-687200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:686600-687200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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