Variant report

Variant	nsv1010881
Chromosome Location	chr4:54471545-54494983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:270)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:54474886-54475092	GM12878	blood:	n/a	n/a
2	BHLHE40	chr4:54474936-54475077	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:54492084-54492423	HepG2	liver:	n/a	n/a
4	CEBPB	chr4:54492243-54492251	K562	blood:	n/a	n/a
5	CEBPB	chr4:54492099-54492413	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:54488852-54489417	IMR90	lung:	n/a	chr4:54489049-54489060
7	CEBPB	chr4:54488960-54489350	Hela-S3	cervix:	n/a	chr4:54489049-54489060
8	CEBPB	chr4:54493424-54493721	H1-hESC	embryonic stem cell:	n/a	chr4:54493567-54493580 chr4:54493567-54493580
9	CEBPB	chr4:54492207-54492326	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:54489037-54489161	HepG2	liver:	n/a	chr4:54489049-54489060
11	CHD2	chr4:54482752-54482779	GM12878	blood:	n/a	n/a
12	CTCF	chr4:54487265-54487526	MCF-7	breast:	n/a	n/a
13	CTCF	chr4:54487340-54487490	A549	lung:	n/a	n/a
14	CTCF	chr4:54487200-54487350	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr4:54487340-54487490	GM12872	blood:	n/a	n/a
16	CTCF	chr4:54487320-54487470	AG04449	skin:	n/a	n/a
17	CTCF	chr4:54487199-54487579	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:54487342-54487442	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr4:54487202-54487570	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr4:54487340-54487490	Caco-2	colon:	n/a	n/a
21	CTCF	chr4:54480992-54481031	GM10266	blood:	n/a	n/a
22	CTCF	chr4:54487360-54487510	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr4:54487367-54487452	A549	lung:	n/a	n/a
24	CTCF	chr4:54487320-54487470	HMF	breast:	n/a	n/a
25	CTCF	chr4:54487340-54487490	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr4:54480956-54481001	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr4:54480919-54481060	IMR90	lung:	n/a	n/a
28	CTCF	chr4:54487363-54487506	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:54480942-54481061	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr4:54480900-54481050	A549	lung:	n/a	n/a
31	CTCF	chr4:54480847-54481111	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:54487280-54487430	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr4:54487400-54487550	BE2_C	brain:	n/a	n/a
34	CTCF	chr4:54487260-54487410	GM12874	blood:	n/a	n/a
35	CTCF	chr4:54487300-54487450	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:54480946-54481050	GM19238	blood:	n/a	n/a
37	CTCF	chr4:54487280-54487430	RPTEC	kidney:	n/a	n/a
38	CTCF	chr4:54487300-54487450	GM12866	blood:	n/a	n/a
39	CTCF	chr4:54487320-54487470	AG09309	skin:	n/a	n/a
40	CTCF	chr4:54480860-54481010	HAc	cerebellar:	n/a	n/a
41	CTCF	chr4:54487299-54487479	Gliobla	brain:	n/a	n/a
42	CTCF	chr4:54487320-54487470	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr4:54487373-54487434	HepG2	liver:	n/a	n/a
44	CTCF	chr4:54480940-54481090	BE2_C	brain:	n/a	n/a
45	CTCF	chr4:54480860-54481010	AG10803	skin:	n/a	n/a
46	CTCF	chr4:54487380-54487530	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr4:54480896-54481096	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:54487400-54487550	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr4:54487300-54487450	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr4:54487282-54487504	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:54487027-54487077	BJ	skin:	n/a
2	chr4:54487027-54487077	AG09319	gingival:	n/a
3	chr4:54487027-54487077	HIPEpiC	eye:	n/a
4	chr4:54487027-54487077	H1-hESC	embryonic stem cell:	embryo
5	chr4:54487027-54487077	HCM	heart:	n/a
6	chr4:54487027-54487077	SKMC	muscle:	n/a
7	chr4:54493964-54494014	GM12891	blood:	n/a
8	chr4:54493964-54494014	HCM	heart:	n/a
9	chr4:54493964-54494014	H1-hESC	embryonic stem cell:	embryo
10	chr4:54487027-54487077	AoSMC	blood vessel:	n/a
11	chr4:54493964-54494014	AG09309	skin:	n/a
12	chr4:54493964-54494014	NH-A	brain:	n/a
13	chr4:54487027-54487077	HepG2	liver:	n/a
14	chr4:54493964-54494014	HL-60	blood:	n/a
15	chr4:54487027-54487077	HCT-116	colon:	n/a
16	chr4:54493964-54494014	HIPEpiC	eye:	n/a
17	chr4:54493964-54494014	HEEpiC	esophagus:	n/a
18	chr4:54487027-54487077	SAEC	small airway:	n/a
19	chr4:54487027-54487077	MCF-7	breast:	n/a
20	chr4:54493964-54494014	Caco-2	colon:	n/a
21	chr4:54487027-54487077	HRCEpiC	kidney:	n/a
22	chr4:54493964-54494014	A549	lung:	n/a
23	chr4:54493964-54494014	ovcar-3	ovarian:	n/a
24	chr4:54487027-54487077	AG04449	skin:	fetal
25	chr4:54493964-54494014	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:54487027-54487077	IMR90	lung:	fetal
27	chr4:54487027-54487077	HCF	heart:	n/a
28	chr4:54493964-54494014	HMEC	breast:	n/a
29	chr4:54487027-54487077	AG04450	lung:	fetal
30	chr4:54487027-54487077	GM06990	blood:	n/a
31	chr4:54493964-54494014	Jurkat	blood:	n/a
32	chr4:54487027-54487077	HUVEC	blood vessel:	n/a
33	chr4:54493964-54494014	BJ	skin:	n/a
34	chr4:54487027-54487077	T-47D	breast:	n/a
35	chr4:54493964-54494014	BE2_C	brain:	n/a
36	chr4:54487027-54487077	AG09309	skin:	n/a
37	chr4:54487027-54487077	GM12891	blood:	n/a
38	chr4:54493964-54494014	K562	blood:	n/a
39	chr4:54487027-54487077	NH-A	brain:	n/a
40	chr4:54493964-54494014	PrEC	prostate:	n/a
41	chr4:54493964-54494014	SK-N-MC	brain:	n/a
42	chr4:54493964-54494014	HRE	kidney:	n/a
43	chr4:54493964-54494014	HepG2	liver:	n/a
44	chr4:54487027-54487077	NHBE	bronchial:	n/a
45	chr4:54493964-54494014	GM19239	blood:	n/a
46	chr4:54487027-54487077	PFSK-1	brain:	n/a
47	chr4:54487027-54487077	GM12892	blood:	n/a
48	chr4:54493964-54494014	IMR90	lung:	fetal
49	chr4:54487027-54487077	K562	blood:	n/a
50	chr4:54487027-54487077	HCPEpiC	choroid plexus:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:54486968..54487480-chr4:54567881..54568820,2	MCF-7	breast:
2	chr4:54484339..54487023-chr4:54487533..54490368,2	K562	blood:
3	chr4:54469447..54472212-chr4:54474648..54477613,2	K562	blood:
4	chr4:54480528..54481474-chr4:54522217..54523059,3	MCF-7	breast:
5	chr4:54487031..54487605-chr4:55099358..55100201,3	MCF-7	breast:
6	chr4:54484339..54487023-chr4:54487533..54490368,2	K562	blood:
7	chr4:54063102..54064001-chr4:54480545..54481508,2	K562	blood:
8	chr4:54469447..54472212-chr4:54474648..54477613,2	K562	blood:
9	chr4:54371855..54372509-chr4:54481038..54481545,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSX2-3	chr4:54469704-54471548	NONHSAT096402

No data

Variant related genes	Relation type
LNX1	TF binding region
LNX1	CpG island

Extended variants
information (count: 635 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74714929	chr4:54471573-54471574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150286885	chr4:54471580-54471581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185655025	chr4:54471592-54471593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76150571	chr4:54471610-54471611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532741401	chr4:54471634-54471635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35335159	chr4:54471641-54471642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570713511	chr4:54471643-54471644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376403086	chr4:54471651-54471652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569356172	chr4:54471652-54471653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2668568	chr4:54471672-54471673	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs548618923	chr4:54471724-54471725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568427241	chr4:54471749-54471750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533959779	chr4:54471804-54471805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553847275	chr4:54471805-54471806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547952741	chr4:54471806-54471807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539547691	chr4:54471808-54471809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145862081	chr4:54471816-54471817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73250975	chr4:54471817-54471818	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs544478755	chr4:54471841-54471842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2616435	chr4:54471842-54471843	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs188332185	chr4:54471843-54471844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540270358	chr4:54471918-54471919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78236582	chr4:54471921-54471922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180678186	chr4:54471939-54471940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532200635	chr4:54471979-54471980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545606155	chr4:54471981-54471982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563066417	chr4:54472070-54472071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184020222	chr4:54472090-54472091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563704578	chr4:54472104-54472105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548842534	chr4:54472173-54472174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188410030	chr4:54472176-54472177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527670791	chr4:54472181-54472182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138502595	chr4:54472226-54472227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116743508	chr4:54472227-54472228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577385049	chr4:54472231-54472232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539513625	chr4:54472245-54472246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556415782	chr4:54472246-54472247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553506377	chr4:54472249-54472250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370440021	chr4:54472260-54472261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569009317	chr4:54472275-54472276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182056806	chr4:54472284-54472285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370769248	chr4:54472297-54472298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574742182	chr4:54472322-54472323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565742301	chr4:54472366-54472367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78679231	chr4:54472374-54472375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113783745	chr4:54472810-54472811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372578709	chr4:54472814-54472815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533198964	chr4:54472816-54472817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550242422	chr4:54472817-54472818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59254887	chr4:54472821-54472822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
Gastrointestinal stromal cancer	17527083	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17209131	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54463800-54471800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:54470600-54471800	Enhancers	Placenta	Placenta
3	chr4:54471800-54472400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:54472800-54473400	Weak transcription	Right Ventricle	heart
5	chr4:54474800-54475400	ZNF genes & repeats	GM12878-XiMat	blood
6	chr4:54480600-54480800	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr4:54480600-54481800	Enhancers	Fetal Intestine Large	intestine
8	chr4:54481400-54481800	Enhancers	Pancreas	Pancrea
9	chr4:54481800-54482600	Weak transcription	Pancreas	Pancrea
10	chr4:54481800-54484600	Weak transcription	Fetal Intestine Large	intestine
11	chr4:54482600-54482800	Enhancers	Pancreas	Pancrea
12	chr4:54482600-54483000	Enhancers	Small Intestine	intestine
13	chr4:54482800-54484600	Weak transcription	Pancreas	Pancrea
14	chr4:54483200-54483800	ZNF genes & repeats	GM12878-XiMat	blood
15	chr4:54483200-54484600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:54484600-54484800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:54484600-54484800	Enhancers	Pancreas	Pancrea
18	chr4:54484600-54485000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr4:54484600-54485000	Enhancers	Fetal Intestine Large	intestine
20	chr4:54484600-54485200	Enhancers	Esophagus	oesophagus
21	chr4:54484800-54487800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr4:54485200-54505800	Weak transcription	Esophagus	oesophagus
23	chr4:54485400-54486400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:54485600-54485800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:54485600-54486000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:54486200-54486800	Enhancers	Brain Germinal Matrix	brain
27	chr4:54486400-54486800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:54486800-54489600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:54487200-54487600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:54487600-54488200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:54487800-54489600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr4:54488200-54488400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:54488200-54489400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:54488400-54488600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:54488400-54488800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:54488400-54488800	Enhancers	Hela-S3	cervix
37	chr4:54488400-54488800	Enhancers	Osteobl	bone
38	chr4:54488400-54489000	Enhancers	HMEC	breast
39	chr4:54488400-54489600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:54488600-54488800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:54488600-54489000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:54488600-54489400	Enhancers	NHDF-Ad	bronchial
43	chr4:54488600-54489600	Enhancers	Placenta	Placenta
44	chr4:54488800-54489400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:54489400-54490600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:54489400-54490800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:54489600-54492600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:54489600-54492600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:54489600-54495800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:54490600-54491000	Enhancers	Ovary	ovary

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