Variant report

Variant	nsv878587
Chromosome Location	chr4:8031471-8075134
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:976)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:8052351-8052437	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr4:8039082-8039561	GM12878	blood:	n/a	n/a
3	BCL3	chr4:8048544-8049032	GM12878	blood:	n/a	chr4:8049002-8049011
4	BCL3	chr4:8051760-8052130	GM12878	blood:	n/a	n/a
5	BCL3	chr4:8048580-8049026	GM12878	blood:	n/a	chr4:8049002-8049011
6	BCL3	chr4:8051772-8052024	GM12878	blood:	n/a	n/a
7	BCL3	chr4:8038912-8039504	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:8042424-8042710	K562	blood:	n/a	n/a
9	BHLHE40	chr4:8069388-8069707	K562	blood:	n/a	n/a
10	BHLHE40	chr4:8042425-8042692	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:8052547-8052963	HepG2	liver:	n/a	n/a
12	BHLHE40	chr4:8052473-8052834	HepG2	liver:	n/a	n/a
13	CBX3	chr4:8065639-8066235	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:8065744-8066192	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:8065778-8066062	K562	blood:	n/a	n/a
16	CBX3	chr4:8065798-8065980	K562	blood:	n/a	n/a
17	CEBPB	chr4:8058752-8058940	HepG2	liver:	n/a	chr4:8058881-8058892
18	CEBPB	chr4:8055589-8055789	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:8034949-8035108	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:8058783-8058947	HepG2	liver:	n/a	chr4:8058881-8058892
21	CEBPD	chr4:8052511-8052966	HepG2	liver:	n/a	n/a
22	CHD2	chr4:8051122-8051443	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr4:8049980-8049988	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr4:8052164-8052523	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr4:8048823-8048827	GM12878	blood:	n/a	n/a
26	CHD2	chr4:8060181-8060187	HepG2	liver:	n/a	n/a
27	CTCF	chr4:8037260-8037410	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr4:8047600-8047750	NB4	blood:	n/a	n/a
29	CTCF	chr4:8063010-8063107	H1-hESC	embryonic stem cell:	n/a	chr4:8063079-8063089
30	CTCF	chr4:8039852-8039902	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:8047758-8047824	A549	lung:	n/a	n/a
32	CTCF	chr4:8052520-8052670	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr4:8054365-8054447	H1-hESC	embryonic stem cell:	n/a	chr4:8054399-8054408
34	CTCF	chr4:8036787-8036833	GM19239	blood:	n/a	n/a
35	CTCF	chr4:8037280-8037430	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr4:8039850-8039927	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr4:8047700-8047850	HepG2	liver:	n/a	n/a
38	CTCF	chr4:8037340-8037490	AG09309	skin:	n/a	n/a
39	CTCF	chr4:8047720-8047870	A549	lung:	n/a	n/a
40	CTCF	chr4:8036142-8036227	GM19239	blood:	n/a	n/a
41	CTCF	chr4:8047680-8047830	Caco-2	colon:	n/a	n/a
42	CTCF	chr4:8034980-8035130	GM12871	blood:	n/a	n/a
43	CTCF	chr4:8047720-8047870	HepG2	liver:	n/a	n/a
44	CTCF	chr4:8032220-8032370	HMEC	breast:	n/a	n/a
45	CTCF	chr4:8032059-8032099	NHEK	skin:	n/a	n/a
46	CTCF	chr4:8037280-8037430	HMEC	breast:	n/a	n/a
47	CTCF	chr4:8037280-8037430	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr4:8037370-8037401	GM19239	blood:	n/a	n/a
49	CTCF	chr4:8047764-8047834	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr4:8063880-8064030	WERI-Rb-1	eye:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8062478-8062528	BE2_C	brain:	n/a
2	chr4:8074092-8074142	U87	brain:	n/a
3	chr4:8062478-8062528	SKMC	muscle:	n/a
4	chr4:8071003-8071053	PFSK-1	brain:	n/a
5	chr4:8037325-8037375	NHBE	bronchial:	n/a
6	chr4:8050781-8050831	HEEpiC	esophagus:	n/a
7	chr4:8062478-8062528	HRE	kidney:	n/a
8	chr4:8074092-8074142	ovcar-3	ovarian:	n/a
9	chr4:8046793-8046843	Hela-S3	cervix:	n/a
10	chr4:8037325-8037375	HIPEpiC	eye:	n/a
11	chr4:8062590-8062640	PANC-1	pancreas:	n/a
12	chr4:8071486-8071536	HRCEpiC	kidney:	n/a
13	chr4:8074092-8074142	RPTEC	kidney:	n/a
14	chr4:8062478-8062528	MCF10A-Er-Src	breast:	n/a
15	chr4:8037325-8037375	Jurkat	blood:	n/a
16	chr4:8062590-8062640	HIPEpiC	eye:	n/a
17	chr4:8062478-8062528	HCM	heart:	n/a
18	chr4:8071202-8071252	AG09319	gingival:	n/a
19	chr4:8037325-8037375	GM12892	blood:	n/a
20	chr4:8046793-8046843	NB4	blood:	n/a
21	chr4:8062541-8062591	Hela-S3	cervix:	n/a
22	chr4:8062590-8062640	NH-A	brain:	n/a
23	chr4:8050781-8050831	AG09309	skin:	n/a
24	chr4:8071202-8071252	HUVEC	blood vessel:	n/a
25	chr4:8062478-8062528	HMEC	breast:	n/a
26	chr4:8034100-8034150	PrEC	prostate:	n/a
27	chr4:8073790-8073840	NH-A	brain:	n/a
28	chr4:8062541-8062591	SK-N-MC	brain:	n/a
29	chr4:8034100-8034150	NB4	blood:	n/a
30	chr4:8071486-8071536	ProgFib	skin:	n/a
31	chr4:8062541-8062591	HUVEC	blood vessel:	n/a
32	chr4:8034100-8034150	HAEpiC	amniotic membrane:	n/a
33	chr4:8062541-8062591	GM12891	blood:	n/a
34	chr4:8046547-8046597	GM12878	blood:	n/a
35	chr4:8071003-8071053	AoSMC	blood vessel:	n/a
36	chr4:8034100-8034150	GM12878	blood:	n/a
37	chr4:8071486-8071536	HCT-116	colon:	n/a
38	chr4:8071003-8071053	HRPEpiC	eye:	n/a
39	chr4:8073804-8073854	SKMC	muscle:	n/a
40	chr4:8071202-8071252	HIPEpiC	eye:	n/a
41	chr4:8034100-8034150	GM12892	blood:	n/a
42	chr4:8073790-8073840	HRE	kidney:	n/a
43	chr4:8046793-8046843	SAEC	small airway:	n/a
44	chr4:8071003-8071053	HCPEpiC	choroid plexus:	n/a
45	chr4:8074092-8074142	MCF10A-Er-Src	breast:	n/a
46	chr4:8074192-8074242	HMEC	breast:	n/a
47	chr4:8071202-8071252	Caco-2	colon:	n/a
48	chr4:8074192-8074242	AG09309	skin:	n/a
49	chr4:8074192-8074242	GM12891	blood:	n/a
50	chr4:8050781-8050831	PFSK-1	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:
2	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
3	chr4:8030886..8034532-chr4:8039153..8041983,3	MCF-7	breast:
4	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:
5	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
6	chr4:8030886..8034532-chr4:8039153..8041983,3	MCF-7	breast:
7	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
8	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
9	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:
10	chr4:8024330..8026063-chr4:8034890..8037450,2	MCF-7	breast:
11	chr4:8030441..8032567-chr4:8033404..8037009,3	K562	blood:
12	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
13	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
14	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:
15	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:
16	chr4:8027811..8029629-chr4:8031244..8032843,2	K562	blood:
17	chr4:8030441..8032567-chr4:8033404..8037009,3	K562	blood:
18	chr4:8019333..8020892-chr4:8033325..8035259,2	MCF-7	breast:
19	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3TC1-2	chr4:8068787-8069451	ENSG00000251460.1
2	lnc-SH3TC1-2	chr4:8068255-8068448	ENSG00000251460.1

No data

Variant related genes	Relation type
ABLIM2	TF binding region
ENSG00000251460	TF binding region
ABLIM2	CpG island
ENSG00000251460	CpG island
ENSG00000273267	chromatin interactions

Extended variants
information (count: 2314 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2314 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2385904	chr4:8031471-8031472	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371414088	chr4:8031474-8031475	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111255429	chr4:8031487-8031488	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536197433	chr4:8031488-8031489	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374578092	chr4:8031501-8031502	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557699481	chr4:8031508-8031509	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539342093	chr4:8031523-8031524	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182628821	chr4:8031539-8031540	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199626550	chr4:8031540-8031541	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548889717	chr4:8031570-8031571	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11942146	chr4:8031590-8031591	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575429795	chr4:8031597-8031598	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541117326	chr4:8031628-8031629	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557667758	chr4:8031659-8031660	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112306043	chr4:8031672-8031673	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146485299	chr4:8031683-8031684	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541377633	chr4:8031686-8031687	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1320072	chr4:8031693-8031694	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187758352	chr4:8031704-8031705	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530799896	chr4:8031735-8031736	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552122146	chr4:8031739-8031740	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564285480	chr4:8031770-8031771	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528627363	chr4:8031821-8031822	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374052959	chr4:8031836-8031837	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568527393	chr4:8031854-8031855	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529310602	chr4:8031856-8031857	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546124361	chr4:8031857-8031858	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550958033	chr4:8031869-8031870	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576010476	chr4:8031902-8031903	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540101001	chr4:8031923-8031924	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139941166	chr4:8031971-8031972	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567044082	chr4:8032015-8032016	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534086712	chr4:8032044-8032045	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145223167	chr4:8032083-8032084	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564116148	chr4:8032094-8032095	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111792552	chr4:8032140-8032141	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376124645	chr4:8032151-8032152	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370237007	chr4:8032162-8032163	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192759791	chr4:8032179-8032180	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184815178	chr4:8032202-8032203	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541441291	chr4:8032218-8032219	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556525729	chr4:8032219-8032220	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575477054	chr4:8032234-8032235	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149170533	chr4:8032240-8032241	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564169427	chr4:8032270-8032271	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528300571	chr4:8032271-8032272	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79664475	chr4:8032284-8032285	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143219965	chr4:8032302-8032303	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73092349	chr4:8032315-8032316	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559441374	chr4:8032329-8032330	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8010600-8052000	Weak transcription	Left Ventricle	heart
2	chr4:8012400-8039000	Weak transcription	Gastric	stomach
3	chr4:8012800-8035000	Weak transcription	Pancreas	Pancrea
4	chr4:8013000-8036600	Weak transcription	Right Ventricle	heart
5	chr4:8017400-8040400	Weak transcription	Right Atrium	heart
6	chr4:8022000-8037600	Weak transcription	Lung	lung
7	chr4:8022200-8040600	Weak transcription	Fetal Brain Female	brain
8	chr4:8022400-8035400	Weak transcription	Brain Anterior Caudate	brain
9	chr4:8022400-8039000	Weak transcription	Brain Angular Gyrus	brain
10	chr4:8023200-8039600	Weak transcription	Brain Germinal Matrix	brain
11	chr4:8023200-8041000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr4:8023800-8037200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr4:8023800-8041200	Weak transcription	Brain Substantia Nigra	brain
14	chr4:8025800-8031800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr4:8028800-8035600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr4:8029200-8031600	Weak transcription	HSMMtube	muscle
17	chr4:8029200-8031800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:8029200-8035400	Strong transcription	Spleen	Spleen
19	chr4:8029800-8046600	Weak transcription	Brain Hippocampus Middle	brain
20	chr4:8030000-8031800	Weak transcription	Aorta	Aorta
21	chr4:8030400-8039200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr4:8030600-8033800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr4:8030800-8031800	Enhancers	HMEC	breast
24	chr4:8030800-8037600	Weak transcription	Fetal Intestine Small	intestine
25	chr4:8031000-8031600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:8031000-8031600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:8031000-8031800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:8031000-8032000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:8031000-8032200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr4:8031000-8032800	Genic enhancers	Esophagus	oesophagus
31	chr4:8031200-8031600	Enhancers	NHEK	skin
32	chr4:8031200-8032400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:8031200-8032600	Enhancers	Fetal Muscle Leg	muscle
34	chr4:8031200-8032600	Enhancers	HSMM	muscle
35	chr4:8031200-8052000	Weak transcription	Psoas Muscle	Psoas
36	chr4:8031400-8031800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr4:8031400-8032200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:8031400-8032400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:8031400-8032400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:8031400-8032600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:8031400-8033000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
42	chr4:8031400-8033400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
43	chr4:8031600-8031800	Bivalent Enhancer	HepG2	liver
44	chr4:8031600-8031800	Bivalent Enhancer	NH-A	brain
45	chr4:8031600-8032400	Flanking Active TSS	NHEK	skin
46	chr4:8031600-8032600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr4:8031600-8032600	Bivalent Enhancer	Placenta	Placenta
48	chr4:8031600-8032600	Enhancers	HSMMtube	muscle
49	chr4:8031800-8032200	Flanking Active TSS	HMEC	breast
50	chr4:8031800-8033000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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