Variant report

Variant	nsv1004485
Chromosome Location	chr4:121542992-121716769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:874)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:121588574-121588579	K562	blood:	n/a	n/a
2	ARID3A	chr4:121614174-121614541	HepG2	liver:	n/a	n/a
3	ATF2	chr4:121670498-121670947	GM12878	blood:	n/a	n/a
4	BACH1	chr4:121642846-121642911	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:121594017-121594053	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:121640212-121640444	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr4:121670672-121671060	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:121686870-121687098	GM12878	blood:	n/a	n/a
9	BRCA1	chr4:121690199-121690775	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr4:121644141-121644145	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:121651232-121651259	H1-hESC	embryonic stem cell:	n/a	n/a
12	CCNT2	chr4:121573758-121573939	K562	blood:	n/a	n/a
13	CEBPB	chr4:121606939-121607247	HepG2	liver:	n/a	chr4:121607082-121607093
14	CEBPB	chr4:121592716-121593068	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:121631130-121631448	Hela-S3	cervix:	n/a	chr4:121631295-121631306
16	CEBPB	chr4:121606969-121607255	A549	lung:	n/a	chr4:121607082-121607093
17	CEBPB	chr4:121645254-121645513	IMR90	lung:	n/a	chr4:121645385-121645402
18	CEBPB	chr4:121690345-121690783	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:121617954-121618297	Hela-S3	cervix:	n/a	chr4:121617999-121618011
20	CEBPB	chr4:121614196-121614485	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:121614129-121614531	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:121606961-121607243	H1-hESC	embryonic stem cell:	n/a	chr4:121607082-121607093
23	CEBPB	chr4:121613598-121613728	A549	lung:	n/a	n/a
24	CEBPB	chr4:121614175-121614520	A549	lung:	n/a	n/a
25	CEBPB	chr4:121557622-121557676	H1-hESC	embryonic stem cell:	n/a	chr4:121557649-121557662 chr4:121557649-121557660 chr4:121557649-121557662
26	CEBPB	chr4:121631112-121631528	IMR90	lung:	n/a	chr4:121631295-121631306
27	CEBPB	chr4:121614054-121614540	A549	lung:	n/a	n/a
28	CEBPB	chr4:121635451-121636206	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:121614204-121614449	MCF-7	breast:	n/a	n/a
30	CEBPB	chr4:121645169-121646234	Hela-S3	cervix:	n/a	chr4:121645385-121645402 chr4:121645889-121645902 chr4:121645891-121645902 chr4:121645891-121645900
31	CEBPB	chr4:121704092-121704827	IMR90	lung:	n/a	chr4:121704325-121704338 chr4:121704325-121704338 chr4:121704196-121704209
32	CEBPB	chr4:121640171-121640485	MCF-7	breast:	n/a	chr4:121640181-121640192
33	CEBPB	chr4:121643338-121643603	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:121614121-121614530	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:121606918-121607260	IMR90	lung:	n/a	chr4:121607082-121607093
36	CEBPB	chr4:121631141-121631341	HepG2	liver:	n/a	chr4:121631295-121631306
37	CEBPB	chr4:121606955-121607205	Hela-S3	cervix:	n/a	chr4:121607082-121607093
38	CEBPB	chr4:121676743-121677031	HepG2	liver:	n/a	chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676918-121676929
39	CEBPZ	chr4:121610364-121610412	HepG2	liver:	n/a	n/a
40	CHD2	chr4:121670552-121671041	GM12878	blood:	n/a	n/a
41	CHD2	chr4:121690442-121690766	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr4:121655980-121656247	GM12878	blood:	n/a	n/a
43	CTCF	chr4:121614240-121614390	BE2_C	brain:	n/a	n/a
44	CTCF	chr4:121640220-121640370	GM12868	blood:	n/a	n/a
45	CTCF	chr4:121640203-121640443	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:121640220-121640370	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr4:121693220-121693370	BE2_C	brain:	n/a	n/a
48	CTCF	chr4:121640177-121640453	GM19238	blood:	n/a	n/a
49	CTCF	chr4:121614160-121614310	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:121640168-121640455	Fibrobl	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:121613795-121613845	NHBE	bronchial:	n/a
2	chr4:121613795-121613845	HepG2	liver:	n/a
3	chr4:121569769-121569819	H1-hESC	embryonic stem cell:	embryo
4	chr4:121569769-121569819	NH-A	brain:	n/a
5	chr4:121569769-121569819	MCF10A-Er-Src	breast:	n/a
6	chr4:121613795-121613845	GM19239	blood:	n/a
7	chr4:121569769-121569819	HCF	heart:	n/a
8	chr4:121613795-121613845	CMK	blood:	n/a
9	chr4:121569769-121569819	PANC-1	pancreas:	n/a
10	chr4:121613795-121613845	AG09319	gingival:	n/a
11	chr4:121569769-121569819	HCPEpiC	choroid plexus:	n/a
12	chr4:121613795-121613845	SK-N-SH	brain:	n/a
13	chr4:121569769-121569819	GM12892	blood:	n/a
14	chr4:121569769-121569819	SK-N-SH	brain:	n/a
15	chr4:121613795-121613845	SAEC	small airway:	n/a
16	chr4:121569769-121569819	SK-N-MC	brain:	n/a
17	chr4:121569769-121569819	HRE	kidney:	n/a
18	chr4:121613795-121613845	K562	blood:	n/a
19	chr4:121569769-121569819	NHDF-neo	bronchial:	n/a
20	chr4:121569769-121569819	HRCEpiC	kidney:	n/a
21	chr4:121569769-121569819	CMK	blood:	n/a
22	chr4:121613795-121613845	SKMC	muscle:	n/a
23	chr4:121569769-121569819	SAEC	small airway:	n/a
24	chr4:121569769-121569819	HNPCEpiC	eye:	n/a
25	chr4:121569769-121569819	SK-N-SH_RA	brain:	n/a
26	chr4:121613795-121613845	U87	brain:	n/a
27	chr4:121569769-121569819	AG04450	lung:	fetal
28	chr4:121569769-121569819	NT2-D1	testis:	n/a
29	chr4:121613795-121613845	NH-A	brain:	n/a
30	chr4:121613795-121613845	PrEC	prostate:	n/a
31	chr4:121613795-121613845	HIPEpiC	eye:	n/a
32	chr4:121613795-121613845	ProgFib	skin:	n/a
33	chr4:121569769-121569819	RPTEC	kidney:	n/a
34	chr4:121613795-121613845	SK-N-MC	brain:	n/a
35	chr4:121569769-121569819	NHBE	bronchial:	n/a
36	chr4:121613795-121613845	BJ	skin:	n/a
37	chr4:121569769-121569819	ProgFib	skin:	n/a
38	chr4:121569769-121569819	Caco-2	colon:	n/a
39	chr4:121569769-121569819	PrEC	prostate:	n/a
40	chr4:121569769-121569819	Hepatocyte	liver:	n/a
41	chr4:121613795-121613845	AG09309	skin:	n/a
42	chr4:121613795-121613845	T-47D	breast:	n/a
43	chr4:121613795-121613845	RPTEC	kidney:	n/a
44	chr4:121613795-121613845	HAEpiC	amniotic membrane:	n/a
45	chr4:121613795-121613845	GM12892	blood:	n/a
46	chr4:121613795-121613845	Hela-S3	cervix:	n/a
47	chr4:121569769-121569819	MCF-7	breast:	n/a
48	chr4:121613795-121613845	ovcar-3	ovarian:	n/a
49	chr4:121613795-121613845	HRPEpiC	eye:	n/a
50	chr4:121613795-121613845	Hepatocyte	liver:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:121639899..121640642-chr4:121840005..121841112,3	MCF-7	breast:
2	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:
3	chr4:121646983..121649694-chr4:121650404..121652066,2	K562	blood:
4	chr4:121561336..121562974-chr4:121568163..121571035,2	MCF-7	breast:
5	chr4:121396849..121398573-chr4:121700140..121702182,2	K562	blood:
6	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
7	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:
8	chr4:121575389..121577725-chr4:121580963..121583228,2	K562	blood:
9	chr4:121593641..121594483-chr9:126875138..126875779,2	MCF-7	breast:
10	chr4:121574015..121575886-chr4:121579540..121581895,2	MCF-7	breast:
11	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:
12	chr4:121646983..121649694-chr4:121650404..121652066,2	K562	blood:
13	chr4:121574015..121575886-chr4:121579540..121581895,2	MCF-7	breast:
14	chr4:121622815..121625386-chr4:121625794..121628188,2	K562	blood:
15	chr4:121622815..121625386-chr4:121625794..121628188,2	K562	blood:
16	chr4:121575389..121577725-chr4:121580963..121583228,2	K562	blood:
17	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
18	chr4:121077068..121077961-chr4:121639964..121640817,3	MCF-7	breast:
19	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:
20	chr4:121561336..121562974-chr4:121568163..121571035,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC079341.1-4	chr4:121571662-121571943	XLOC_003671
2	lnc-AC079341.1-4	chr4:121560264-121560506	XLOC_003671
3	lnc-AC079341.1-4	chr4:121571665-121571951	XLOC_003671
4	lnc-AC079341.1-4	chr4:121560245-121560506	XLOC_003671

No data

Variant related genes	Relation type
PRDM5	TF binding region
ENSG00000249409	TF binding region
PRDM5	CpG island
ENSG00000249409	CpG island
ELAVL4	miRNA target sites
ELF3	miRNA target sites

Extended variants
information (count: 6032 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6032 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148465933	chr4:121554601-121554602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565265728	chr4:121554610-121554611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs58568085	chr4:121554638-121554639	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs74885785	chr4:121554733-121554734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141732810	chr4:121554765-121554766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192912581	chr4:121554772-121554773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561247957	chr4:121554785-121554786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147226272	chr4:121554807-121554808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201582026	chr4:121554825-121554826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200521843	chr4:121554826-121554827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116668382	chr4:121554827-121554828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563881657	chr4:121554852-121554853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532529050	chr4:121554858-121554859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185127919	chr4:121554913-121554914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548905496	chr4:121554956-121554957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565981043	chr4:121554970-121554971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528493372	chr4:121555021-121555022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs80346801	chr4:121555035-121555036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76717333	chr4:121555036-121555037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545256771	chr4:121555176-121555177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77669429	chr4:121555183-121555184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537471287	chr4:121555190-121555191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536522718	chr4:121555217-121555218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556112992	chr4:121555245-121555246	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs13121457	chr4:121555267-121555268	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs538392637	chr4:121555275-121555276	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs558615011	chr4:121555276-121555277	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs79941565	chr4:121555294-121555295	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs187927371	chr4:121555296-121555297	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs144477747	chr4:121555331-121555332	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs574818533	chr4:121555340-121555341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138985527	chr4:121555352-121555353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149915895	chr4:121555372-121555373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532729881	chr4:121555455-121555456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192491773	chr4:121555560-121555561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550875183	chr4:121555578-121555579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13149724	chr4:121555612-121555613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs528560469	chr4:121555652-121555653	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs548623745	chr4:121555678-121555679	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs369310634	chr4:121555701-121555702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1353469	chr4:121555706-121555707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs144946514	chr4:121555736-121555737	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs35922095	chr4:121555738-121555739	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs569795007	chr4:121555742-121555743	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs538828875	chr4:121555788-121555789	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs558424437	chr4:121555809-121555810	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs377662964	chr4:121555833-121555834	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs534387933	chr4:121555834-121555835	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs554175628	chr4:121555889-121555890	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs574081856	chr4:121555904-121555905	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121554600-121555400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr4:121555400-121557200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:121555800-121556400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:121556400-121557600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr4:121557200-121557800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:121557200-121558600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:121557600-121557800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:121560000-121560400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr4:121560800-121561800	Enhancers	Fetal Heart	heart
10	chr4:121568200-121569600	Weak transcription	Aorta	Aorta
11	chr4:121568800-121569200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:121569200-121569600	Active TSS	H1 Cell Line	embryonic stem cell
13	chr4:121569200-121569600	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr4:121569200-121569600	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr4:121569200-121569600	Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr4:121569200-121569600	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr4:121569200-121569800	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr4:121569200-121569800	Active TSS	H9 Cell Line	embryonic stem cell
19	chr4:121569200-121570200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:121569600-121569800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
21	chr4:121569600-121569800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr4:121569600-121569800	Strong transcription	Aorta	Aorta
23	chr4:121569600-121570000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:121569600-121570000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr4:121569600-121570000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr4:121569600-121570000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:121569600-121570200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:121569800-121570000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr4:121569800-121570000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr4:121569800-121570000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr4:121569800-121570000	ZNF genes & repeats	Aorta	Aorta
32	chr4:121569800-121570200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:121570000-121570400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:121570000-121570400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:121570000-121570400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:121570000-121577400	Weak transcription	Aorta	Aorta
37	chr4:121570200-121570600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:121570600-121571000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:121577400-121577600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:121577400-121577800	ZNF genes & repeats	Aorta	Aorta
41	chr4:121577800-121580800	Weak transcription	Aorta	Aorta
42	chr4:121579400-121579800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:121579400-121580800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr4:121579600-121580600	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr4:121579600-121580800	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr4:121579600-121581000	Enhancers	Primary hematopoietic stem cells	blood
47	chr4:121579800-121580000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:121579800-121580400	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr4:121579800-121580400	Enhancers	Fetal Stomach	stomach
50	chr4:121579800-121580400	Enhancers	Monocytes-CD14+_RO01746	blood

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