Variant report

Variant	esv3428482
Chromosome Location	chr4:651252-655450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:427)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:652831-653271	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:652747-653269	HepG2	liver:	n/a	n/a
3	CBX3	chr4:651182-651820	K562	blood:	n/a	n/a
4	CEBPZ	chr4:652988-653024	HepG2	liver:	n/a	n/a
5	CHD2	chr4:652751-652986	HepG2	liver:	n/a	n/a
6	CTCF	chr4:653260-653410	HepG2	liver:	n/a	n/a
7	CTCF	chr4:653300-653450	HepG2	liver:	n/a	n/a
8	EP300	chr4:652811-653280	HepG2	liver:	n/a	n/a
9	EP300	chr4:652790-653234	HepG2	liver:	n/a	n/a
10	EP300	chr4:653681-653803	HepG2	liver:	n/a	n/a
11	FOXA1	chr4:652671-653343	HepG2	liver:	n/a	n/a
12	FOXA1	chr4:652740-653259	HepG2	liver:	n/a	n/a
13	FOXA1	chr4:652691-653262	HepG2	liver:	n/a	n/a
14	FOXA1	chr4:652659-653376	HepG2	liver:	n/a	n/a
15	FOXA2	chr4:652853-653231	HepG2	liver:	n/a	n/a
16	FOXA2	chr4:652511-653380	HepG2	liver:	n/a	n/a
17	HNF4A	chr4:652893-653264	HepG2	liver:	n/a	n/a
18	JUND	chr4:652890-653227	HepG2	liver:	n/a	n/a
19	JUND	chr4:652814-653201	HepG2	liver:	n/a	n/a
20	MAX	chr4:652724-653576	HepG2	liver:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:652843-652852 chr4:653434-653444 chr4:653412-653422
21	MAX	chr4:653180-653624	NB4	blood:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
22	MAX	chr4:653136-653620	H1-hESC	embryonic stem cell:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
23	MAX	chr4:653155-653512	A549	lung:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
24	MAX	chr4:652437-653567	HepG2	liver:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:652843-652852 chr4:653434-653444 chr4:653412-653422
25	MAX	chr4:653155-653698	HUVEC	blood vessel:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
26	MXI1	chr4:652723-653579	HepG2	liver:	n/a	n/a
27	MYBL2	chr4:652653-653326	HepG2	liver:	n/a	n/a
28	MYC	chr4:652989-653050	HepG2	liver:	n/a	n/a
29	MYC	chr4:652923-652987	HepG2	liver:	n/a	n/a
30	MYC	chr4:652883-652921	HepG2	liver:	n/a	n/a
31	NFIC	chr4:652755-653269	HepG2	liver:	n/a	n/a
32	NR2C2	chr4:653286-653799	GM12878	blood:	n/a	n/a
33	NR2C2	chr4:651264-652307	HepG2	liver:	n/a	n/a
34	NR2F2	chr4:651325-652481	HepG2	liver:	n/a	n/a
35	NR2F2	chr4:651086-652523	MCF-7	breast:	n/a	n/a
36	NR2F2	chr4:651092-652404	K562	blood:	n/a	n/a
37	NR2F2	chr4:651430-652489	HepG2	liver:	n/a	n/a
38	NR2F2	chr4:651141-652387	K562	blood:	n/a	n/a
39	POLR2A	chr4:652768-652813	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr4:653127-653856	Raji	blood:	n/a	n/a
41	POLR2A	chr4:651350-651665	GM12878	blood:	n/a	n/a
42	POLR2A	chr4:651472-651644	GM12878	blood:	n/a	n/a
43	POLR2A	chr4:653142-653544	GM12878	blood:	n/a	n/a
44	POLR2A	chr4:653308-653419	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr4:652589-652650	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr4:651983-652308	GM12878	blood:	n/a	n/a
47	POLR2A	chr4:651842-652079	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:653558-655042	K562	blood:	n/a	n/a
49	POLR2A	chr4:651884-652383	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr4:653707-653902	GM12878	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:653615-653665	PANC-1	pancreas:	n/a
2	chr4:652823-652873	HepG2	liver:	n/a
3	chr4:652702-652752	AG09309	skin:	n/a
4	chr4:652702-652752	AG09319	gingival:	n/a
5	chr4:652891-652941	LNCaP	prostate:	n/a
6	chr4:652751-652801	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:652702-652752	RPTEC	kidney:	n/a
8	chr4:652823-652873	HEEpiC	esophagus:	n/a
9	chr4:652891-652941	Hepatocyte	liver:	n/a
10	chr4:652891-652941	K562	blood:	n/a
11	chr4:652823-652873	Jurkat	blood:	n/a
12	chr4:652907-652957	K562	blood:	n/a
13	chr4:652823-652873	Hepatocyte	liver:	n/a
14	chr4:653615-653665	SK-N-SH	brain:	n/a
15	chr4:652823-652873	PFSK-1	brain:	n/a
16	chr4:652751-652801	T-47D	breast:	n/a
17	chr4:652907-652957	HNPCEpiC	eye:	n/a
18	chr4:652527-652577	Jurkat	blood:	n/a
19	chr4:652702-652752	ProgFib	skin:	n/a
20	chr4:652751-652801	ovcar-3	ovarian:	n/a
21	chr4:653615-653665	HCPEpiC	choroid plexus:	n/a
22	chr4:652702-652752	U87	brain:	n/a
23	chr4:653615-653665	NT2-D1	testis:	n/a
24	chr4:653615-653665	HRE	kidney:	n/a
25	chr4:652823-652873	HIPEpiC	eye:	n/a
26	chr4:652823-652873	ovcar-3	ovarian:	n/a
27	chr4:652907-652957	SKMC	muscle:	n/a
28	chr4:652891-652941	HNPCEpiC	eye:	n/a
29	chr4:652751-652801	SAEC	small airway:	n/a
30	chr4:652907-652957	PANC-1	pancreas:	n/a
31	chr4:653615-653665	PrEC	prostate:	n/a
32	chr4:653615-653665	AoSMC	blood vessel:	n/a
33	chr4:652527-652577	NB4	blood:	n/a
34	chr4:652702-652752	LNCaP	prostate:	n/a
35	chr4:652907-652957	SK-N-SH_RA	brain:	n/a
36	chr4:652751-652801	NHDF-neo	bronchial:	n/a
37	chr4:652891-652941	SAEC	small airway:	n/a
38	chr4:652702-652752	HAEpiC	amniotic membrane:	n/a
39	chr4:652527-652577	SK-N-SH	brain:	n/a
40	chr4:652891-652941	AG09309	skin:	n/a
41	chr4:652751-652801	HCM	heart:	n/a
42	chr4:652907-652957	NT2-D1	testis:	n/a
43	chr4:653615-653665	HUVEC	blood vessel:	n/a
44	chr4:652527-652577	HepG2	liver:	n/a
45	chr4:652907-652957	ECC-1	luminal epithelium:	n/a
46	chr4:652702-652752	BJ	skin:	n/a
47	chr4:652823-652873	HCT-116	colon:	n/a
48	chr4:652907-652957	HRE	kidney:	n/a
49	chr4:652702-652752	T-47D	breast:	n/a
50	chr4:652907-652957	AG09319	gingival:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:641525..644066-chr4:652058..654958,2	K562	blood:
2	chr4:613849..616261-chr4:650426..653017,2	K562	blood:
3	chr4:644162..647846-chr4:649268..652076,4	MCF-7	breast:
4	chr4:647827..650169-chr4:651801..653823,2	K562	blood:
5	chr11:116512208..116512892-chr4:653530..654530,4	MCF-7	breast:
6	chr4:649938..652851-chr4:653641..657433,6	K562	blood:
7	chr4:646849..649113-chr4:654761..657491,3	K562	blood:
8	chr4:642131..644821-chr4:649750..652284,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5I-5	chr4:655335-655487	NONHSAT094591
2	lnc-ATP5I-5	chr4:654998-655734	ENSG00000272927.1

No data

Variant related genes	Relation type
ENSG00000242686	TF binding region
PDE6B	TF binding region
ENSG00000242686	CpG island
PDE6B	CpG island
ENSG00000272927	chromatin interactions
ENSG00000133256	chromatin interactions
ENSG00000242686	chromatin interactions

Extended variants
information (count: 283 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574676553	chr4:651252-651253	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs541985727	chr4:651256-651257	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs368069770	chr4:651257-651258	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs560334464	chr4:651266-651267	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs369946269	chr4:651268-651269	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs113246945	chr4:651287-651288	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs201623488	chr4:651288-651289	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs537010934	chr4:651290-651291	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs531652183	chr4:651291-651292	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs550223936	chr4:651298-651299	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs202051878	chr4:651299-651300	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs370241561	chr4:651301-651302	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs200492958	chr4:651308-651309	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs112079685	chr4:651311-651312	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs200233700	chr4:651323-651324	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs368553268	chr4:651325-651326	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs539705144	chr4:651335-651336	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs557807682	chr4:651336-651337	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs28742266	chr4:651369-651370	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs563385251	chr4:651371-651372	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs530816505	chr4:651393-651394	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs112810432	chr4:651415-651416	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573372565	chr4:651416-651417	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs540730000	chr4:651417-651418	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs553905863	chr4:651425-651426	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs546133194	chr4:651462-651463	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs564039825	chr4:651473-651474	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs572343320	chr4:651485-651486	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs528093606	chr4:651493-651494	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs546471591	chr4:651508-651509	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs377079022	chr4:651509-651510	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs369721659	chr4:651516-651517	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564652243	chr4:651517-651518	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs372600702	chr4:651520-651521	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs190882084	chr4:651529-651530	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs531718830	chr4:651539-651540	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs543419461	chr4:651550-651551	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs377244180	chr4:651563-651564	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs28478159	chr4:651609-651610	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs547921786	chr4:651610-651611	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs565872477	chr4:651622-651623	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533027972	chr4:651623-651624	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551632210	chr4:651629-651630	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569815502	chr4:651632-651633	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs116534205	chr4:651676-651677	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs113260926	chr4:651679-651680	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
47	rs529025357	chr4:651681-651682	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs373027908	chr4:651714-651715	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534401743	chr4:651715-651716	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs552694017	chr4:651728-651729	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:631400-657000	Weak transcription	Right Atrium	heart
2	chr4:641800-657000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:642200-652800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr4:642400-654600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:642800-657000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:643000-657000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:645800-656800	Weak transcription	Gastric	stomach
8	chr4:648400-657000	Weak transcription	Right Ventricle	heart
9	chr4:648800-653400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:649000-652800	Weak transcription	Brain Germinal Matrix	brain
11	chr4:649200-652800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr4:649200-653000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:649800-653200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:649800-655600	Weak transcription	Thymus	Thymus
15	chr4:650000-653200	Weak transcription	Fetal Brain Female	brain
16	chr4:650000-654000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:650000-654200	Enhancers	HepG2	liver
18	chr4:650200-652800	Weak transcription	Brain Substantia Nigra	brain
19	chr4:650600-652600	Weak transcription	Brain Anterior Caudate	brain
20	chr4:650600-652800	Weak transcription	Brain Angular Gyrus	brain
21	chr4:650800-652800	Weak transcription	Primary T cells from cord blood	blood
22	chr4:650800-656000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr4:651000-651400	Enhancers	Pancreas	Pancrea
24	chr4:651000-652800	Weak transcription	Brain Hippocampus Middle	brain
25	chr4:651000-653200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr4:651000-653600	Weak transcription	Fetal Brain Male	brain
27	chr4:651200-651400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:651200-652200	Enhancers	Spleen	Spleen
29	chr4:651200-653200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr4:651200-654400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:651400-653000	Enhancers	Lung	lung
32	chr4:651400-653200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:651400-653200	Weak transcription	Dnd41	blood
34	chr4:651400-653400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr4:651400-656400	Weak transcription	Pancreas	Pancrea
36	chr4:651600-651800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr4:651600-653200	Weak transcription	Fetal Intestine Small	intestine
38	chr4:651600-657000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr4:651600-657200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr4:651800-653200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr4:651800-656800	Weak transcription	Primary B cells from cord blood	blood
42	chr4:652000-653600	Weak transcription	Fetal Stomach	stomach
43	chr4:652000-656800	Weak transcription	Fetal Lung	lung
44	chr4:652200-654000	Genic enhancers	Spleen	Spleen
45	chr4:652400-655200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr4:652400-656800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr4:652600-654000	Strong transcription	Brain Anterior Caudate	brain
48	chr4:652600-656800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:652600-656800	Weak transcription	Fetal Thymus	thymus
50	chr4:652800-653600	Strong transcription	Primary T cells from cord blood	blood

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