Variant report

Variant	nsv594955
Chromosome Location	chr4:102935902-103008712
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:102939394-102939672	A549	lung:	n/a	chr4:102939534-102939547 chr4:102939535-102939546 chr4:102939534-102939547 chr4:102939534-102939545
2	CEBPB	chr4:102964493-102964648	K562	blood:	n/a	chr4:102964520-102964531
3	CEBPB	chr4:102962532-102962662	H1-hESC	embryonic stem cell:	n/a	chr4:102962623-102962634 chr4:102962622-102962639 chr4:102962623-102962636
4	CEBPB	chr4:102958722-102958968	HepG2	liver:	n/a	n/a
5	CEBPB	chr4:102958729-102958881	A549	lung:	n/a	n/a
6	CEBPB	chr4:102939368-102939687	HepG2	liver:	n/a	chr4:102939534-102939547 chr4:102939535-102939546 chr4:102939534-102939547 chr4:102939534-102939545
7	CEBPB	chr4:103007318-103007577	HepG2	liver:	n/a	chr4:103007450-103007461
8	CEBPB	chr4:102939386-102939722	IMR90	lung:	n/a	chr4:102939534-102939547 chr4:102939535-102939546 chr4:102939534-102939547 chr4:102939534-102939545
9	CEBPB	chr4:102939444-102939574	H1-hESC	embryonic stem cell:	n/a	chr4:102939534-102939547 chr4:102939535-102939546 chr4:102939534-102939547 chr4:102939534-102939545
10	CEBPB	chr4:102964391-102964639	IMR90	lung:	n/a	chr4:102964520-102964531
11	CEBPB	chr4:102997869-102998165	A549	lung:	n/a	n/a
12	CEBPB	chr4:102969012-102969231	HepG2	liver:	n/a	chr4:102969164-102969175 chr4:102969113-102969126 chr4:102969113-102969126 chr4:102969113-102969124 chr4:102969113-102969124 chr4:102969114-102969125
13	CEBPB	chr4:103007377-103007553	A549	lung:	n/a	chr4:103007450-103007461
14	CEBPB	chr4:102958713-102958975	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:103007322-103007591	IMR90	lung:	n/a	chr4:103007450-103007461
16	CEBPB	chr4:102964419-102964628	HepG2	liver:	n/a	chr4:102964520-102964531
17	CEBPB	chr4:102964001-102964893	Hela-S3	cervix:	n/a	chr4:102964520-102964531
18	CTCF	chr4:102977080-102977230	BE2_C	brain:	n/a	n/a
19	CTCF	chr4:102977080-102977230	GM12873	blood:	n/a	n/a
20	CTCF	chr4:102977080-102977230	HMF	breast:	n/a	n/a
21	CTCF	chr4:102977040-102977190	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr4:102977060-102977210	GM12864	blood:	n/a	n/a
23	CTCF	chr4:102977120-102977270	HCT-116	colon:	n/a	n/a
24	CTCF	chr4:102977040-102977190	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr4:102977080-102977230	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr4:102977220-102977370	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr4:102959732-102959794	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:102977100-102977250	HMEC	breast:	n/a	n/a
29	CTCF	chr4:102977060-102977210	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr4:102977180-102977330	HCT-116	colon:	n/a	n/a
31	CTCF	chr4:102976980-102977130	AG04450	lung:	n/a	n/a
32	CTCF	chr4:102977320-102977470	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr4:102977120-102977390	HMEC	breast:	n/a	n/a
34	CTCF	chr4:102977000-102977150	AG09319	gingival:	n/a	n/a
35	CTCF	chr4:102977100-102977250	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:102977060-102977210	HEK293	kidney:	n/a	n/a
37	CTCF	chr4:102977180-102977330	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr4:102977120-102977270	HVMF	connective:	n/a	n/a
39	CTCF	chr4:102977120-102977270	GM12872	blood:	n/a	n/a
40	CTCF	chr4:103006381-103006456	GM10266	blood:	n/a	n/a
41	CTCF	chr4:102977200-102977350	RPTEC	kidney:	n/a	n/a
42	CTCF	chr4:102977120-102977270	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:102977088-102977234	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr4:102977240-102977390	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr4:102976980-102977130	GM12864	blood:	n/a	n/a
46	CTCF	chr4:102977120-102977370	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr4:102977060-102977210	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr4:102977100-102977250	SAEC	small airway:	n/a	n/a
49	CTCF	chr4:102977040-102977190	HMF	breast:	n/a	n/a
50	CTCF	chr4:102977220-102977370	HCFaa	heart:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102995477-102995527	HMEC	breast:	n/a
2	chr4:102995477-102995527	AG09319	gingival:	n/a
3	chr4:102995477-102995527	ProgFib	skin:	n/a
4	chr4:102995477-102995527	SAEC	small airway:	n/a
5	chr4:102995477-102995527	HCT-116	colon:	n/a
6	chr4:102995477-102995527	A549	lung:	n/a
7	chr4:102995477-102995527	Jurkat	blood:	n/a
8	chr4:102995477-102995527	HUVEC	blood vessel:	n/a
9	chr4:102995477-102995527	HRCEpiC	kidney:	n/a
10	chr4:102995477-102995527	T-47D	breast:	n/a
11	chr4:102995477-102995527	ECC-1	luminal epithelium:	n/a
12	chr4:102995477-102995527	Hepatocyte	liver:	n/a
13	chr4:102995477-102995527	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:102995477-102995527	SK-N-MC	brain:	n/a
15	chr4:102995477-102995527	GM12892	blood:	n/a
16	chr4:102995477-102995527	NT2-D1	testis:	n/a
17	chr4:102995477-102995527	NHDF-neo	bronchial:	n/a
18	chr4:102995477-102995527	HRE	kidney:	n/a
19	chr4:102995477-102995527	LNCaP	prostate:	n/a
20	chr4:102995477-102995527	Caco-2	colon:	n/a
21	chr4:102995477-102995527	Hela-S3	cervix:	n/a
22	chr4:102995477-102995527	MCF-7	breast:	n/a
23	chr4:102995477-102995527	GM12878	blood:	n/a
24	chr4:102995477-102995527	HL-60	blood:	n/a
25	chr4:102995477-102995527	GM19239	blood:	n/a
26	chr4:102995477-102995527	HRPEpiC	eye:	n/a
27	chr4:102995477-102995527	HNPCEpiC	eye:	n/a
28	chr4:102995477-102995527	AG04449	skin:	fetal
29	chr4:102995477-102995527	HCM	heart:	n/a
30	chr4:102995477-102995527	AG10803	skin:	n/a
31	chr4:102995477-102995527	AoSMC	blood vessel:	n/a
32	chr4:102995477-102995527	ovcar-3	ovarian:	n/a
33	chr4:102995477-102995527	MCF10A-Er-Src	breast:	n/a
34	chr4:102995477-102995527	K562	blood:	n/a
35	chr4:102995477-102995527	H1-hESC	embryonic stem cell:	embryo
36	chr4:102995477-102995527	NB4	blood:	n/a
37	chr4:102995477-102995527	AG09309	skin:	n/a
38	chr4:102995477-102995527	IMR90	lung:	fetal
39	chr4:102995477-102995527	PrEC	prostate:	n/a
40	chr4:102995477-102995527	HCPEpiC	choroid plexus:	n/a
41	chr4:102995477-102995527	BJ	skin:	n/a
42	chr4:102995477-102995527	PFSK-1	brain:	n/a
43	chr4:102995477-102995527	PANC-1	pancreas:	n/a
44	chr4:102995477-102995527	HEK293	kidney:	embryo
45	chr4:102995477-102995527	AG04450	lung:	fetal
46	chr4:102995477-102995527	HIPEpiC	eye:	n/a
47	chr4:102995477-102995527	RPTEC	kidney:	n/a
48	chr4:102995477-102995527	GM06990	blood:	n/a
49	chr4:102995477-102995527	U87	brain:	n/a
50	chr4:102995477-102995527	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:102983408..102985207-chr4:102988825..102991000,2	MCF-7	breast:
2	chr4:102929581..102932403-chr4:102937190..102939421,2	K562	blood:
3	chr4:102983408..102985207-chr4:102988825..102991000,2	MCF-7	breast:
4	chr1:173794005..173794756-chr4:102954358..102954878,2	Hela-S3	cervix:
5	chr4:103006830..103008574-chr4:103015934..103018544,2	K562	blood:
6	chr4:102984591..102987150-chr4:102995563..102997735,2	MCF-7	breast:
7	chr17:56735383..56737967-chr4:102987580..102990239,2	MCF-7	breast:
8	chr4:102926272..102927803-chr4:102933320..102936106,2	K562	blood:
9	chr4:102984591..102987150-chr4:102995563..102997735,2	MCF-7	breast:
10	chr4:102935717..102937290-chr4:102939556..102941946,2	K562	blood:
11	chr4:102935717..102937290-chr4:102939556..102941946,2	K562	blood:
12	chr4:102951568..102953598-chr4:102955632..102958106,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC39A8-2	chr4:102953366-102953539	ENSG00000251309.1
2	lnc-NFKB1-5	chr4:102995162-102995377	NONHSAT097576
3	lnc-NFKB1-5	chr4:102994841-102994905	NONHSAT097576
4	lnc-NFKB1-5	chr4:102992432-102992461	NONHSAT097576
5	lnc-NFKB1-5	chr4:102993502-102993557	NONHSAT097576
6	lnc-NFKB1-5	chr4:102982573-102984295	NONHSAT097576
7	lnc-SLC39A8-2	chr4:102957839-102958060	ENSG00000251309.1

No data

Variant related genes	Relation type
BANK1	TF binding region
ENSG00000251309	TF binding region
BANK1	CpG island
ENSG00000251309	CpG island
ENSG00000251309	chromatin interactions
ENSG00000202077	chromatin interactions

Extended variants
information (count: 2281 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2281 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3135465	chr4:102935902-102935903	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572105542	chr4:102935957-102935958	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180907451	chr4:102935984-102935985	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546310778	chr4:102936016-102936017	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565885181	chr4:102936049-102936050	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368946811	chr4:102936075-102936076	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539653036	chr4:102936159-102936160	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138546922	chr4:102936162-102936163	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376563961	chr4:102936165-102936166	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551647331	chr4:102936205-102936206	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570298415	chr4:102936232-102936233	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143187828	chr4:102936311-102936312	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537433134	chr4:102936337-102936338	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114714559	chr4:102936396-102936397	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557539973	chr4:102936531-102936532	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6844449	chr4:102936592-102936593	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs535095873	chr4:102936605-102936606	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148103675	chr4:102936611-102936612	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577872030	chr4:102936672-102936673	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185464429	chr4:102936727-102936728	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557291789	chr4:102936738-102936739	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575481718	chr4:102936767-102936768	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141850630	chr4:102936770-102936771	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72931986	chr4:102936781-102936782	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs528092339	chr4:102936811-102936812	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150602351	chr4:102936817-102936818	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564676507	chr4:102936839-102936840	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533343670	chr4:102936847-102936848	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549013507	chr4:102936860-102936861	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551586413	chr4:102936887-102936888	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570315356	chr4:102936889-102936890	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531079640	chr4:102936915-102936916	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549675087	chr4:102936947-102936948	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17031862	chr4:102936972-102936973	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs190365006	chr4:102937040-102937041	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139688677	chr4:102937044-102937045	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567299892	chr4:102937091-102937092	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571818455	chr4:102937174-102937175	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6845846	chr4:102937196-102937197	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182486047	chr4:102937202-102937203	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575417988	chr4:102937293-102937294	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542509436	chr4:102937344-102937345	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149336942	chr4:102937405-102937406	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146266865	chr4:102937446-102937447	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539886702	chr4:102937520-102937521	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564614562	chr4:102937525-102937526	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532111948	chr4:102937526-102937527	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564451532	chr4:102937653-102937654	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542910190	chr4:102937685-102937686	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543919835	chr4:102937697-102937698	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	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
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102929400-102939800	Strong transcription	Primary B cells from peripheral blood	blood
2	chr4:102932400-102940000	Strong transcription	Primary B cells from cord blood	blood
3	chr4:102938400-102938800	Enhancers	Adipose Nuclei	Adipose
4	chr4:102938400-102953600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr4:102938600-102946400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:102939800-102942800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr4:102940000-102942600	Weak transcription	Primary B cells from cord blood	blood
8	chr4:102942600-102947600	Strong transcription	Primary B cells from cord blood	blood
9	chr4:102942600-102958600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:102942800-102951000	Strong transcription	Primary B cells from peripheral blood	blood
11	chr4:102943000-102944000	Enhancers	HUVEC	blood vessel
12	chr4:102943400-102943800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:102946400-102947400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:102947400-102957800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:102947600-102948400	Weak transcription	Primary B cells from cord blood	blood
16	chr4:102948400-102965400	Strong transcription	Primary B cells from cord blood	blood
17	chr4:102951000-102951800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
18	chr4:102951800-102979200	Strong transcription	Primary B cells from peripheral blood	blood
19	chr4:102955200-102955600	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr4:102955600-102957000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr4:102956200-102958200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:102957000-102957600	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr4:102957000-102958200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:102957000-102958600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr4:102957200-102958000	Enhancers	Psoas Muscle	Psoas
26	chr4:102957600-102957800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:102957600-102957800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr4:102957600-102958200	Enhancers	Fetal Muscle Leg	muscle
29	chr4:102957600-102958800	Enhancers	HSMM	muscle
30	chr4:102957800-102958200	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr4:102957800-102958400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:102957800-102958400	Enhancers	NHDF-Ad	bronchial
33	chr4:102957800-102959000	Enhancers	HSMMtube	muscle
34	chr4:102958200-102958400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr4:102958400-102958600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:102958400-102958600	Enhancers	Adipose Nuclei	Adipose
37	chr4:102958400-102959000	Active TSS	Liver	Liver
38	chr4:102958400-102959000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr4:102958400-102983600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:102958600-102958800	Active TSS	Monocytes-CD14+_RO01746	blood
41	chr4:102958600-102959000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:102958600-102959000	Active TSS	GM12878-XiMat	blood
43	chr4:102958800-102959000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr4:102958800-102959200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr4:102959000-102959200	Enhancers	Liver	Liver
46	chr4:102959000-102959200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr4:102959000-102959800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr4:102959800-102961000	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr4:102963800-102964600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:102963800-102965200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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