Variant report

Variant	nsv594580
Chromosome Location	chr4:69629425-69706273
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	ARID3A	chr4:69637663-69637849	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69683102-69684193	HepG2	liver:	n/a	chr4:69683103-69683119
3	ARID3A	chr4:69662896-69663031	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69680934-69681903	HepG2	liver:	n/a	n/a
5	BHLHE40	chr4:69681403-69681779	HepG2	liver:	n/a	n/a
6	BRCA1	chr4:69667559-69667568	GM12878	blood:	n/a	n/a
7	CEBPB	chr4:69685477-69685793	HepG2	liver:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
8	CEBPB	chr4:69685586-69685776	H1-hESC	embryonic stem cell:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
9	CEBPB	chr4:69685580-69685738	A549	lung:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
10	CEBPB	chr4:69637609-69637853	HepG2	liver:	n/a	chr4:69637743-69637754
11	CEBPB	chr4:69681485-69681922	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:69655534-69655732	HepG2	liver:	n/a	chr4:69655582-69655593 chr4:69655582-69655591
13	CEBPB	chr4:69681686-69681867	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:69684015-69684280	IMR90	lung:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
15	CEBPB	chr4:69684063-69684187	K562	blood:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
16	CEBPB	chr4:69684002-69684205	A549	lung:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
17	CEBPB	chr4:69683737-69684291	HepG2	liver:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
18	CEBPB	chr4:69678841-69679067	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:69685485-69685717	K562	blood:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
20	CEBPB	chr4:69643053-69643196	HepG2	liver:	n/a	chr4:69643169-69643180 chr4:69643170-69643181 chr4:69643169-69643182 chr4:69643169-69643182 chr4:69643169-69643182
21	CEBPB	chr4:69637597-69637887	HepG2	liver:	n/a	chr4:69637743-69637754
22	CEBPB	chr4:69685492-69685778	IMR90	lung:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
23	CEBPB	chr4:69662855-69663059	HepG2	liver:	n/a	chr4:69662889-69662902 chr4:69662889-69662902
24	CEBPD	chr4:69681639-69681887	HepG2	liver:	n/a	n/a
25	CTCF	chr4:69639965-69640014	GM13976	blood:	n/a	n/a
26	CTCF	chr4:69664302-69664340	GM10248	blood:	n/a	n/a
27	CTCF	chr4:69692957-69692997	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr4:69667480-69667630	GM12875	blood:	n/a	n/a
29	CTCF	chr4:69667461-69667559	GM13977	blood:	n/a	n/a
30	CTCF	chr4:69636620-69636770	HPF	lung:	n/a	n/a
31	CTCF	chr4:69639520-69639670	GM06990	blood:	n/a	n/a
32	CTCF	chr4:69683829-69683943	Lung_OC	lung:	n/a	n/a
33	CTCF	chr4:69667445-69667544	GM12892	blood:	n/a	n/a
34	CTCF	chr4:69667538-69667565	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:69667380-69667530	GM12865	blood:	n/a	n/a
36	CTCF	chr4:69661994-69662139	Medullo	brain:	n/a	n/a
37	CTCF	chr4:69667468-69667528	GM12878	blood:	n/a	n/a
38	CTCF	chr4:69667460-69667610	GM12865	blood:	n/a	n/a
39	CTCF	chr4:69667455-69667460	GM12878	blood:	n/a	n/a
40	CTCF	chr4:69645878-69645948	ProgFib	skin:	n/a	n/a
41	CTCF	chr4:69667433-69667636	GM12878	blood:	n/a	n/a
42	CTCF	chr4:69667540-69667690	GM12874	blood:	n/a	n/a
43	CTCF	chr4:69664163-69664241	GM20000	blood:	n/a	n/a
44	CTCF	chr4:69667420-69667614	GM19238	blood:	n/a	n/a
45	CTCF	chr4:69667454-69667458	GM12891	blood:	n/a	n/a
46	CTCF	chr4:69667483-69667568	GM13976	blood:	n/a	n/a
47	CTCF	chr4:69669990-69670027	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr4:69681974-69682009	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr4:69667460-69667562	GM19240	blood:	n/a	n/a
50	CTCF	chr4:69675017-69675085	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69681824-69681874	BE2_C	brain:	n/a
2	chr4:69681824-69681874	NT2-D1	testis:	n/a
3	chr4:69681824-69681874	NHDF-neo	bronchial:	n/a
4	chr4:69681824-69681874	Caco-2	colon:	n/a
5	chr4:69681824-69681874	RPTEC	kidney:	n/a
6	chr4:69681824-69681874	GM12891	blood:	n/a
7	chr4:69681824-69681874	MCF-7	breast:	n/a
8	chr4:69681824-69681874	NH-A	brain:	n/a
9	chr4:69681824-69681874	AG10803	skin:	n/a
10	chr4:69681824-69681874	GM12878	blood:	n/a
11	chr4:69681824-69681874	CMK	blood:	n/a
12	chr4:69681824-69681874	LNCaP	prostate:	n/a
13	chr4:69681824-69681874	HCF	heart:	n/a
14	chr4:69681824-69681874	SKMC	muscle:	n/a
15	chr4:69681824-69681874	MCF10A-Er-Src	breast:	n/a
16	chr4:69681824-69681874	A549	lung:	n/a
17	chr4:69681824-69681874	HEK293	kidney:	embryo
18	chr4:69681824-69681874	SAEC	small airway:	n/a
19	chr4:69681824-69681874	SK-N-SH_RA	brain:	n/a
20	chr4:69681824-69681874	Hela-S3	cervix:	n/a
21	chr4:69681824-69681874	PFSK-1	brain:	n/a
22	chr4:69681824-69681874	ovcar-3	ovarian:	n/a
23	chr4:69681824-69681874	HRE	kidney:	n/a
24	chr4:69681824-69681874	HMEC	breast:	n/a
25	chr4:69681824-69681874	Hepatocyte	liver:	n/a
26	chr4:69681824-69681874	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:69681824-69681874	HRCEpiC	kidney:	n/a
28	chr4:69681824-69681874	PrEC	prostate:	n/a
29	chr4:69681824-69681874	HepG2	liver:	n/a
30	chr4:69681824-69681874	HL-60	blood:	n/a
31	chr4:69681824-69681874	SK-N-SH	brain:	n/a
32	chr4:69681824-69681874	IMR90	lung:	fetal
33	chr4:69681824-69681874	T-47D	breast:	n/a
34	chr4:69681824-69681874	HAEpiC	amniotic membrane:	n/a
35	chr4:69681824-69681874	GM12892	blood:	n/a
36	chr4:69681824-69681874	GM06990	blood:	n/a
37	chr4:69681824-69681874	HRPEpiC	eye:	n/a
38	chr4:69681824-69681874	GM19239	blood:	n/a
39	chr4:69681824-69681874	HCM	heart:	n/a
40	chr4:69681824-69681874	K562	blood:	n/a
41	chr4:69681824-69681874	NHBE	bronchial:	n/a
42	chr4:69681824-69681874	ECC-1	luminal epithelium:	n/a
43	chr4:69681824-69681874	PANC-1	pancreas:	n/a
44	chr4:69681824-69681874	HUVEC	blood vessel:	n/a
45	chr4:69681824-69681874	HIPEpiC	eye:	n/a
46	chr4:69681824-69681874	U87	brain:	n/a
47	chr4:69681824-69681874	HEEpiC	esophagus:	n/a
48	chr4:69681824-69681874	AG04450	lung:	fetal
49	chr4:69681824-69681874	AG09319	gingival:	n/a
50	chr4:69681824-69681874	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:69627049..69629916-chr4:69637911..69640559,2	K562	blood:
2	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
3	chr4:69627049..69629916-chr4:69637911..69640559,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B10-1	chr4:69679713-69680445	NONHSAT096742

Variant related genes	Relation type
ENSG00000251236	TF binding region
ENSG00000250376	TF binding region
UGT2B10	TF binding region
ENSG00000251424	TF binding region
ENSG00000251236	CpG island
ENSG00000250376	CpG island
UGT2B10	CpG island
ENSG00000251424	CpG island

Extended variants
information (count: 2583 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2583 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574215395	chr4:69632024-69632025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543226818	chr4:69632031-69632032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372648619	chr4:69632033-69632034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573330135	chr4:69632145-69632146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567907147	chr4:69632150-69632151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142511919	chr4:69632155-69632156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545133295	chr4:69632207-69632208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145059943	chr4:69632209-69632210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565242753	chr4:69632226-69632227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138907771	chr4:69632249-69632250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185348453	chr4:69632260-69632261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567648239	chr4:69632263-69632264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369733819	chr4:69632291-69632292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142039270	chr4:69632311-69632312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs983346	chr4:69632325-69632326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569629303	chr4:69632386-69632387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116592574	chr4:69632394-69632395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs983347	chr4:69632428-69632429	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs190437835	chr4:69632466-69632467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534313516	chr4:69632488-69632489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554683269	chr4:69632492-69632493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574562099	chr4:69632514-69632515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561280895	chr4:69632541-69632542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543263629	chr4:69632549-69632550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556761180	chr4:69632590-69632591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530309936	chr4:69632596-69632597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545670700	chr4:69632601-69632602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182169213	chr4:69632602-69632603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113636703	chr4:69632650-69632651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117950861	chr4:69632653-69632654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576016963	chr4:69632693-69632694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116686797	chr4:69632736-69632737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561462851	chr4:69632741-69632742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113123452	chr4:69632755-69632756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560510598	chr4:69632757-69632758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530098571	chr4:69632773-69632774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113727683	chr4:69632785-69632786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184952307	chr4:69632800-69632801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562444612	chr4:69632855-69632856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569462897	chr4:69632897-69632898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113201303	chr4:69632908-69632909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9993883	chr4:69632909-69632910	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs188251559	chr4:69632921-69632922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377096374	chr4:69632950-69632951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10034195	chr4:69632988-69632989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs74668230	chr4:69633057-69633058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199931128	chr4:69633060-69633061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376145388	chr4:69633085-69633086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534641311	chr4:69633087-69633088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72848040	chr4:69633094-69633095	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

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
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	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69632000-69637200	Weak transcription	HepG2	liver
2	chr4:69637200-69638200	Enhancers	HepG2	liver
3	chr4:69639000-69643200	Weak transcription	Fetal Intestine Large	intestine
4	chr4:69639400-69640000	ZNF genes & repeats	Fetal Intestine Small	intestine
5	chr4:69640000-69645200	Weak transcription	Fetal Intestine Small	intestine
6	chr4:69645200-69646000	ZNF genes & repeats	Fetal Intestine Small	intestine
7	chr4:69647800-69649400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:69649400-69650000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:69650000-69650600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:69658000-69658200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:69662200-69662400	Enhancers	Rectal Smooth Muscle	rectum
12	chr4:69662400-69663000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr4:69662400-69663800	Enhancers	Liver	Liver
14	chr4:69662800-69664000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:69663000-69663800	Enhancers	Rectal Smooth Muscle	rectum
16	chr4:69663000-69664000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:69663000-69664000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:69663000-69664200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:69663200-69663400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr4:69663200-69663800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:69663200-69664000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:69663400-69663800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr4:69663600-69664000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:69663800-69664400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:69668400-69670000	Enhancers	Fetal Intestine Small	intestine
26	chr4:69669400-69673000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:69670400-69671000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr4:69670600-69671200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:69671000-69671200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:69671200-69673000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr4:69673000-69673600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:69673600-69674000	Enhancers	Liver	Liver
33	chr4:69676600-69678000	Enhancers	HepG2	liver
34	chr4:69678000-69678400	Weak transcription	HepG2	liver
35	chr4:69678400-69679200	Enhancers	HepG2	liver
36	chr4:69679200-69679600	Weak transcription	HepG2	liver
37	chr4:69679600-69681800	Enhancers	HepG2	liver
38	chr4:69680800-69681200	Enhancers	Liver	Liver
39	chr4:69681000-69682600	Enhancers	A549	lung
40	chr4:69681200-69681800	Weak transcription	Liver	Liver
41	chr4:69681400-69682000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:69681600-69684000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:69681800-69682200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:69681800-69682600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:69681800-69682600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:69681800-69683000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:69681800-69683000	Flanking Active TSS	HepG2	liver
48	chr4:69681800-69684600	Active TSS	Liver	Liver
49	chr4:69682000-69682200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr4:69682200-69682400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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