Variant report

Variant	nsv880669
Chromosome Location	chr4:187297232-187382294
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	chr4:187356907-187357919	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr4:187354074-187354310	GM12878	blood:	n/a	n/a
3	BCL3	chr4:187327155-187327407	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:187362735-187362783	K562	blood:	n/a	n/a
5	BRCA1	chr4:187346073-187346283	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr4:187373146-187373490	K562	blood:	n/a	n/a
7	CBX3	chr4:187354461-187354780	K562	blood:	n/a	n/a
8	CBX3	chr4:187373072-187373601	HCT-116	colon:	n/a	n/a
9	CBX3	chr4:187373086-187373652	HCT-116	colon:	n/a	n/a
10	CBX3	chr4:187373144-187373570	K562	blood:	n/a	n/a
11	CCNT2	chr4:187362847-187363236	K562	blood:	n/a	n/a
12	CEBPB	chr4:187371106-187371462	ECC-1	luminal epithelium:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
13	CEBPB	chr4:187371124-187371436	Hela-S3	cervix:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
14	CEBPB	chr4:187378231-187378496	HepG2	liver:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
15	CEBPB	chr4:187371179-187371335	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
16	CEBPB	chr4:187371102-187371494	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
17	CEBPB	chr4:187371122-187371471	A549	lung:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
18	CEBPB	chr4:187325690-187326036	A549	lung:	n/a	n/a
19	CEBPB	chr4:187361057-187361080	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:187360936-187361199	K562	blood:	n/a	n/a
21	CEBPB	chr4:187371108-187371409	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
22	CEBPB	chr4:187371127-187371481	IMR90	lung:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
23	CEBPB	chr4:187379564-187379739	A549	lung:	n/a	n/a
24	CEBPB	chr4:187316995-187317220	K562	blood:	n/a	n/a
25	CEBPB	chr4:187378227-187378457	IMR90	lung:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
26	CEBPB	chr4:187361028-187361112	A549	lung:	n/a	n/a
27	CEBPB	chr4:187378200-187378477	A549	lung:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
28	CEBPB	chr4:187375483-187375595	HepG2	liver:	n/a	chr4:187375528-187375539
29	CEBPB	chr4:187371090-187371490	ECC-1	luminal epithelium:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
30	CEBPB	chr4:187371126-187371469	H1-hESC	embryonic stem cell:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
31	CEBPB	chr4:187371132-187371388	MCF-7	breast:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
32	CEBPB	chr4:187375448-187375609	A549	lung:	n/a	chr4:187375528-187375539
33	CEBPB	chr4:187371144-187371490	HepG2	liver:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
34	CEBPB	chr4:187378219-187378507	K562	blood:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
35	CEBPD	chr4:187362609-187362999	K562	blood:	n/a	n/a
36	CTCF	chr4:187317340-187317490	BE2_C	brain:	n/a	n/a
37	CTCF	chr4:187327206-187327294	GM12891	blood:	n/a	n/a
38	CTCF	chr4:187341108-187341150	Lung_OC	lung:	n/a	n/a
39	CTCF	chr4:187373700-187373850	Caco-2	colon:	n/a	n/a
40	CTCF	chr4:187366164-187366171	LNCaP	prostate:	n/a	n/a
41	CTCF	chr4:187366425-187366465	GM12878	blood:	n/a	n/a
42	CTCF	chr4:187323579-187323630	GM20000	blood:	n/a	n/a
43	CTCF	chr4:187341664-187341704	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:187327408-187327411	GM19239	blood:	n/a	n/a
45	CTCF	chr4:187303140-187303290	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr4:187338795-187338852	GM10248	blood:	n/a	n/a
47	CTCF	chr4:187312960-187313110	GM12873	blood:	n/a	n/a
48	CTCF	chr4:187345580-187345730	A549	lung:	n/a	n/a
49	CTCF	chr4:187372553-187372584	GM13976	blood:	n/a	n/a
50	CTCF	chr4:187327360-187327510	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187360860-187360910	HEEpiC	esophagus:	n/a
2	chr4:187360860-187360910	AoSMC	blood vessel:	n/a
3	chr4:187349665-187349715	AG10803	skin:	n/a
4	chr4:187349665-187349715	ECC-1	luminal epithelium:	n/a
5	chr4:187349665-187349715	AG04450	lung:	fetal
6	chr4:187357928-187357978	HCM	heart:	n/a
7	chr4:187357928-187357978	NHBE	bronchial:	n/a
8	chr4:187349665-187349715	U87	brain:	n/a
9	chr4:187357928-187357978	PrEC	prostate:	n/a
10	chr4:187357928-187357978	AG09309	skin:	n/a
11	chr4:187357928-187357978	AG04450	lung:	fetal
12	chr4:187357928-187357978	HRCEpiC	kidney:	n/a
13	chr4:187357928-187357978	K562	blood:	n/a
14	chr4:187349131-187349181	CMK	blood:	n/a
15	chr4:187360860-187360910	RPTEC	kidney:	n/a
16	chr4:187349131-187349181	MCF10A-Er-Src	breast:	n/a
17	chr4:187349665-187349715	HRE	kidney:	n/a
18	chr4:187349131-187349181	GM12878	blood:	n/a
19	chr4:187360860-187360910	HRCEpiC	kidney:	n/a
20	chr4:187360860-187360910	HUVEC	blood vessel:	n/a
21	chr4:187357928-187357978	HepG2	liver:	n/a
22	chr4:187349131-187349181	ovcar-3	ovarian:	n/a
23	chr4:187360860-187360910	NH-A	brain:	n/a
24	chr4:187349131-187349181	AG10803	skin:	n/a
25	chr4:187349665-187349715	SK-N-MC	brain:	n/a
26	chr4:187357928-187357978	HEK293	kidney:	embryo
27	chr4:187349665-187349715	SK-N-SH	brain:	n/a
28	chr4:187349714-187349764	HMEC	breast:	n/a
29	chr4:187349714-187349764	SK-N-MC	brain:	n/a
30	chr4:187357928-187357978	GM19239	blood:	n/a
31	chr4:187349665-187349715	Jurkat	blood:	n/a
32	chr4:187360860-187360910	HepG2	liver:	n/a
33	chr4:187349665-187349715	Caco-2	colon:	n/a
34	chr4:187357928-187357978	AG10803	skin:	n/a
35	chr4:187349665-187349715	HMEC	breast:	n/a
36	chr4:187349665-187349715	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:187360860-187360910	GM12892	blood:	n/a
38	chr4:187357928-187357978	U87	brain:	n/a
39	chr4:187349714-187349764	MCF10A-Er-Src	breast:	n/a
40	chr4:187360860-187360910	BJ	skin:	n/a
41	chr4:187360860-187360910	NB4	blood:	n/a
42	chr4:187360860-187360910	AG09319	gingival:	n/a
43	chr4:187360860-187360910	CMK	blood:	n/a
44	chr4:187360860-187360910	MCF-7	breast:	n/a
45	chr4:187360860-187360910	AG10803	skin:	n/a
46	chr4:187357928-187357978	HL-60	blood:	n/a
47	chr4:187357928-187357978	GM12892	blood:	n/a
48	chr4:187349131-187349181	AG09319	gingival:	n/a
49	chr4:187357928-187357978	AoSMC	blood vessel:	n/a
50	chr4:187357928-187357978	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187336442..187338955-chr4:187341117..187342706,2	K562	blood:
2	chr4:187363286..187364885-chr4:187368218..187369820,2	K562	blood:
3	chr4:187371013..187372540-chr4:187375746..187378339,2	K562	blood:
4	chr4:187365176..187367106-chr4:187368874..187370492,2	K562	blood:
5	chr4:187367777..187369317-chr4:187372463..187374481,2	MCF-7	breast:
6	chr4:187363385..187366676-chr4:187368218..187370374,3	K562	blood:
7	chr4:187371013..187372540-chr4:187375746..187378339,2	K562	blood:
8	chr4:187327492..187329160-chr4:187332412..187335274,2	K562	blood:
9	chr4:187332850..187335061-chr4:187335595..187338116,3	K562	blood:
10	chr4:187367777..187369317-chr4:187372463..187374481,2	MCF-7	breast:
11	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
12	chr4:187327492..187329160-chr4:187332412..187335274,2	K562	blood:
13	chr4:187332850..187335061-chr4:187335595..187338116,3	K562	blood:
14	chr4:187332246..187335061-chr4:187336434..187338116,2	K562	blood:
15	chr4:187363385..187366676-chr4:187368218..187370374,3	K562	blood:
16	chr4:187336442..187338955-chr4:187341117..187342706,2	K562	blood:
17	chr4:187365176..187367106-chr4:187368874..187370492,2	K562	blood:
18	chr4:187339945..187342685-chr4:187344135..187346623,2	K562	blood:
19	chr4:187363286..187364885-chr4:187368218..187369820,2	K562	blood:
20	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
21	chr4:187332246..187335061-chr4:187336434..187338116,2	K562	blood:
22	chr4:187339945..187342685-chr4:187344135..187346623,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTNR1A-1	chr4:187352772-187352922	NONHSAT099658
2	lnc-MTNR1A-1	chr4:187347391-187348252	ENSG00000251165.1
3	lnc-MTNR1A-1	chr4:187344882-187344986	ENSG00000251165.1
4	lnc-MTNR1A-1	chr4:187349859-187350004	ENSG00000251165.1
5	lnc-MTNR1A-1	chr4:187353299-187353392	ENSG00000251165.1
6	lnc-MTNR1A-1	chr4:187352772-187352922	ENSG00000251165.1
7	lnc-MTNR1A-1	chr4:187348128-187348252	ENSG00000251165.1
8	lnc-MTNR1A-1	chr4:187345244-187345390	ENSG00000251165.1
9	lnc-MTNR1A-1	chr4:187344883-187344986	NONHSAT099658
10	lnc-MTNR1A-1	chr4:187353299-187353392	ENSG00000251165.1
11	lnc-MTNR1A-1	chr4:187344882-187344986	ENSG00000251165.1
12	lnc-MTNR1A-1	chr4:187347391-187348252	NONHSAT099658
13	lnc-MTNR1A-1	chr4:187337280-187337490	NONHSAT099658
14	lnc-MTNR1A-1	chr4:187353299-187353392	NONHSAT099658
15	lnc-MTNR1A-1	chr4:187352772-187352922	ENSG00000251165.1
16	lnc-MTNR1A-1	chr4:187345244-187345390	NONHSAT099658
17	lnc-MTNR1A-1	chr4:187347391-187347447	ENSG00000251165.1

Variant related genes	Relation type
F11-AS1	TF binding region
F11-AS1	CpG island

Extended variants
information (count: 2418 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2418 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540558429	chr4:187303216-187303217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373666157	chr4:187303225-187303226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184807761	chr4:187303229-187303230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111658280	chr4:187303246-187303247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577006390	chr4:187303257-187303258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7675440	chr4:187303264-187303265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370570148	chr4:187303290-187303291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531313983	chr4:187303294-187303295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547846611	chr4:187303296-187303297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10032656	chr4:187303301-187303302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527273061	chr4:187303362-187303363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547718068	chr4:187303375-187303376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189749496	chr4:187303376-187303377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs58856998	chr4:187303378-187303379	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs550112557	chr4:187303427-187303428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181398741	chr4:187303468-187303469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535972505	chr4:187303472-187303473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555873220	chr4:187303479-187303480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550148020	chr4:187303496-187303497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370483010	chr4:187303497-187303498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535004162	chr4:187303530-187303531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375990013	chr4:187303596-187303597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554080469	chr4:187303648-187303649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74786178	chr4:187303692-187303693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143422225	chr4:187303738-187303739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184355715	chr4:187303764-187303765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189156552	chr4:187303783-187303784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143851554	chr4:187303813-187303814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368873089	chr4:187303814-187303815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181810942	chr4:187303825-187303826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148650251	chr4:187303887-187303888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186533671	chr4:187303930-187303931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34656431	chr4:187303944-187303945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6839207	chr4:187303948-187303949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372424114	chr4:187303957-187303958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564065212	chr4:187303982-187303983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533467323	chr4:187303983-187303984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541373404	chr4:187304033-187304034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200886224	chr4:187304051-187304052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190938344	chr4:187304066-187304067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570179257	chr4:187304070-187304071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150675619	chr4:187304096-187304097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139897982	chr4:187304103-187304104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371821564	chr4:187304115-187304116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143768514	chr4:187304147-187304148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533216972	chr4:187304164-187304165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181051455	chr4:187304172-187304173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557875141	chr4:187304234-187304235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571581882	chr4:187304237-187304238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539374009	chr4:187304324-187304325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Acute lymphoblastic leukemia	20067559	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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187303200-187303600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:187303400-187303800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:187303600-187313200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:187313200-187313400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:187313200-187313600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr4:187313200-187313600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:187313200-187313600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:187316800-187317200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr4:187316800-187317600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:187316800-187318000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr4:187317000-187317600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:187325400-187326200	Enhancers	A549	lung
13	chr4:187325600-187326200	Enhancers	Fetal Kidney	kidney
14	chr4:187325800-187326000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:187325800-187326000	Enhancers	Gastric	stomach
16	chr4:187325800-187326200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:187325800-187326200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:187326000-187327000	Weak transcription	Gastric	stomach
19	chr4:187326000-187329200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:187326200-187326800	Active TSS	A549	lung
21	chr4:187326200-187327200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:187326800-187327400	Enhancers	A549	lung
23	chr4:187327000-187327200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:187327000-187327400	Enhancers	Fetal Lung	lung
25	chr4:187327000-187327600	ZNF genes & repeats	Gastric	stomach
26	chr4:187327000-187327600	Enhancers	Pancreas	Pancrea
27	chr4:187327200-187327400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:187327200-187327600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:187327200-187327600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:187334600-187336200	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr4:187334800-187335200	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr4:187334800-187335400	Enhancers	Small Intestine	intestine
33	chr4:187334800-187336200	Enhancers	Duodenum Mucosa	Duodenum
34	chr4:187334800-187336200	Enhancers	Fetal Intestine Large	intestine
35	chr4:187334800-187336200	Enhancers	Fetal Intestine Small	intestine
36	chr4:187335000-187335200	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr4:187335000-187336200	Enhancers	Pancreas	Pancrea
38	chr4:187335200-187335600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
39	chr4:187335200-187335600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr4:187335600-187336200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr4:187335600-187336400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr4:187335800-187336400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:187336200-187339200	Weak transcription	Fetal Intestine Small	intestine
44	chr4:187337800-187338200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:187339200-187340000	Enhancers	Fetal Intestine Small	intestine
46	chr4:187340800-187342400	Enhancers	Fetal Lung	lung
47	chr4:187342400-187343400	Weak transcription	Fetal Lung	lung
48	chr4:187343400-187343600	Enhancers	Fetal Stomach	stomach
49	chr4:187343400-187345400	Enhancers	Fetal Lung	lung
50	chr4:187343600-187343800	Enhancers	Sigmoid Colon	Sigmoid Colon

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