Variant report

Variant	nsv945413
Chromosome Location	chr1:242542299-242607506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:242588617-242588811	HepG2	liver:	n/a	n/a
2	BATF	chr1:242588702-242588830	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:242555256-242555349	A549	lung:	n/a	n/a
4	CBX3	chr1:242588649-242588927	HCT-116	colon:	n/a	n/a
5	CEBPB	chr1:242559279-242559448	HepG2	liver:	n/a	chr1:242559383-242559394 chr1:242559300-242559311
6	CEBPB	chr1:242594283-242594631	K562	blood:	n/a	n/a
7	CEBPB	chr1:242576058-242576317	A549	lung:	n/a	n/a
8	CEBPB	chr1:242590616-242590785	HepG2	liver:	n/a	chr1:242590685-242590696
9	CEBPB	chr1:242590525-242590660	K562	blood:	n/a	n/a
10	CEBPB	chr1:242594276-242594628	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:242594278-242594614	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:242594271-242594619	A549	lung:	n/a	n/a
13	CEBPB	chr1:242588352-242588652	HepG2	liver:	n/a	chr1:242588455-242588466
14	CEBPB	chr1:242559268-242559449	A549	lung:	n/a	chr1:242559383-242559394 chr1:242559300-242559311
15	CTCF	chr1:242588600-242588750	HMF	breast:	n/a	n/a
16	CTCF	chr1:242590171-242590175	GM12878	blood:	n/a	n/a
17	CTCF	chr1:242588640-242588790	GM12870	blood:	n/a	n/a
18	CTCF	chr1:242588620-242588770	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr1:242588580-242588730	GM12873	blood:	n/a	n/a
20	CTCF	chr1:242590120-242590270	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr1:242570933-242571029	GM20000	blood:	n/a	n/a
22	CTCF	chr1:242590124-242590287	Gliobla	brain:	n/a	n/a
23	CTCF	chr1:242590140-242590290	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr1:242588642-242588810	LNCaP	prostate:	n/a	n/a
25	CTCF	chr1:242588712-242588799	GM20000	blood:	n/a	n/a
26	CTCF	chr1:242549719-242549814	Fibrobl	skin:	n/a	n/a
27	CTCF	chr1:242590080-242590230	HEK293	kidney:	n/a	n/a
28	CTCF	chr1:242588739-242588799	GM12892	blood:	n/a	n/a
29	CTCF	chr1:242590140-242590290	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr1:242590060-242590210	HMEC	breast:	n/a	n/a
31	CTCF	chr1:242588620-242588770	GM12872	blood:	n/a	n/a
32	CTCF	chr1:242588718-242588832	NHEK	skin:	n/a	n/a
33	CTCF	chr1:242588625-242588838	GM12878	blood:	n/a	n/a
34	CTCF	chr1:242588722-242588801	GM19239	blood:	n/a	n/a
35	CTCF	chr1:242588680-242588830	GM12874	blood:	n/a	n/a
36	CTCF	chr1:242588680-242588830	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:242590100-242590250	BE2_C	brain:	n/a	n/a
38	CTCF	chr1:242590100-242590250	A549	lung:	n/a	n/a
39	CTCF	chr1:242590130-242590251	GM19240	blood:	n/a	n/a
40	CTCF	chr1:242588660-242588810	GM12864	blood:	n/a	n/a
41	CTCF	chr1:242588620-242588770	HCFaa	heart:	n/a	n/a
42	CTCF	chr1:242583680-242583830	AG10803	skin:	n/a	n/a
43	CTCF	chr1:242588628-242588846	A549	lung:	n/a	n/a
44	CTCF	chr1:242590180-242590330	GM12873	blood:	n/a	n/a
45	CTCF	chr1:242588660-242588810	BE2_C	brain:	n/a	n/a
46	CTCF	chr1:242588460-242588610	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr1:242588660-242588810	GM12873	blood:	n/a	n/a
48	CTCF	chr1:242588660-242588810	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr1:242588720-242588870	NHEK	skin:	n/a	n/a
50	CTCF	chr1:242588700-242588850	GM12871	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242605061-242605111	HEEpiC	esophagus:	n/a
2	chr1:242605061-242605111	AoSMC	blood vessel:	n/a
3	chr1:242605061-242605111	SKMC	muscle:	n/a
4	chr1:242605061-242605111	AG04449	skin:	fetal
5	chr1:242605061-242605111	BE2_C	brain:	n/a
6	chr1:242605061-242605111	HCF	heart:	n/a
7	chr1:242605061-242605111	ovcar-3	ovarian:	n/a
8	chr1:242605061-242605111	RPTEC	kidney:	n/a
9	chr1:242605061-242605111	HCPEpiC	choroid plexus:	n/a
10	chr1:242605061-242605111	GM12891	blood:	n/a
11	chr1:242605061-242605111	AG09319	gingival:	n/a
12	chr1:242605061-242605111	K562	blood:	n/a
13	chr1:242605061-242605111	MCF10A-Er-Src	breast:	n/a
14	chr1:242605061-242605111	IMR90	lung:	fetal
15	chr1:242605061-242605111	T-47D	breast:	n/a
16	chr1:242605061-242605111	SK-N-SH_RA	brain:	n/a
17	chr1:242605061-242605111	Hepatocyte	liver:	n/a
18	chr1:242605061-242605111	SK-N-SH	brain:	n/a
19	chr1:242605061-242605111	MCF-7	breast:	n/a
20	chr1:242605061-242605111	AG09309	skin:	n/a
21	chr1:242605061-242605111	U87	brain:	n/a
22	chr1:242605061-242605111	Hela-S3	cervix:	n/a
23	chr1:242605061-242605111	HIPEpiC	eye:	n/a
24	chr1:242605061-242605111	HCM	heart:	n/a
25	chr1:242605061-242605111	NB4	blood:	n/a
26	chr1:242605061-242605111	HCT-116	colon:	n/a
27	chr1:242605061-242605111	HRPEpiC	eye:	n/a
28	chr1:242605061-242605111	GM06990	blood:	n/a
29	chr1:242605061-242605111	PFSK-1	brain:	n/a
30	chr1:242605061-242605111	PrEC	prostate:	n/a
31	chr1:242605061-242605111	PANC-1	pancreas:	n/a
32	chr1:242605061-242605111	NHBE	bronchial:	n/a
33	chr1:242605061-242605111	SK-N-MC	brain:	n/a
34	chr1:242605061-242605111	LNCaP	prostate:	n/a
35	chr1:242605061-242605111	A549	lung:	n/a
36	chr1:242605061-242605111	AG10803	skin:	n/a
37	chr1:242605061-242605111	GM19239	blood:	n/a
38	chr1:242605061-242605111	NHDF-neo	bronchial:	n/a
39	chr1:242605061-242605111	HEK293	kidney:	embryo
40	chr1:242605061-242605111	HRCEpiC	kidney:	n/a
41	chr1:242605061-242605111	GM12878	blood:	n/a
42	chr1:242605061-242605111	CMK	blood:	n/a
43	chr1:242605061-242605111	BJ	skin:	n/a
44	chr1:242605061-242605111	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:242605061-242605111	SAEC	small airway:	n/a
46	chr1:242605061-242605111	GM12892	blood:	n/a
47	chr1:242605061-242605111	ProgFib	skin:	n/a
48	chr1:242605061-242605111	AG04450	lung:	fetal
49	chr1:242605061-242605111	H1-hESC	embryonic stem cell:	embryo
50	chr1:242605061-242605111	HRE	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:242570206..242572074-chr1:242586277..242589124,2	K562	blood:
2	chr1:242595107..242597872-chr1:242601027..242602558,2	K562	blood:
3	chr1:242594168..242597872-chr1:242601027..242602906,3	K562	blood:
4	chr1:242579229..242580899-chr1:242592362..242595019,2	K562	blood:
5	chr1:242590294..242592687-chr1:242593690..242595305,2	K562	blood:
6	chr1:242595852..242597675-chr1:242599631..242602192,2	MCF-7	breast:
7	chr1:242595107..242597872-chr1:242601027..242602558,2	K562	blood:
8	chr1:242594168..242597872-chr1:242601027..242602906,3	K562	blood:
9	chr1:242595852..242597675-chr1:242599631..242602192,2	MCF-7	breast:
10	chr1:242536607..242538996-chr1:242545702..242547462,2	MCF-7	breast:
11	chr1:242579229..242580899-chr1:242592362..242595019,2	K562	blood:
12	chr1:242183008..242183632-chr1:242588513..242589035,2	MCF-7	breast:
13	chr1:242570206..242572074-chr1:242586277..242589124,2	K562	blood:
14	chr1:242590294..242592687-chr1:242593690..242595305,2	K562	blood:
15	chr1:242576728..242577460-chr2:3592302..3593192,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000213690	TF binding region
ENSG00000213690	CpG island

Extended variants
information (count: 2967 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2967 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150031900	chr1:242542325-242542326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147752504	chr1:242542333-242542334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72763078	chr1:242542378-242542379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs72763079	chr1:242542413-242542414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs546642260	chr1:242542428-242542429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75306418	chr1:242542449-242542450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142655048	chr1:242542450-242542451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368487652	chr1:242542503-242542504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144890207	chr1:242542513-242542514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147773748	chr1:242542515-242542516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536575365	chr1:242542593-242542594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192136013	chr1:242542611-242542612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566584082	chr1:242542618-242542619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372026910	chr1:242542694-242542695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538806485	chr1:242542726-242542727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76209066	chr1:242542742-242542743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542222261	chr1:242542771-242542772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112439337	chr1:242542779-242542780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184504113	chr1:242542853-242542854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554546008	chr1:242542870-242542871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10926708	chr1:242542873-242542874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs540538219	chr1:242542888-242542889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374376263	chr1:242542904-242542905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577392384	chr1:242542921-242542922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs60955446	chr1:242542932-242542933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188533558	chr1:242542980-242542981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147628726	chr1:242543003-242543004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148810945	chr1:242543019-242543020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530627099	chr1:242543040-242543041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544298928	chr1:242543055-242543056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560885391	chr1:242543059-242543060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181341452	chr1:242543091-242543092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143521963	chr1:242543097-242543098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148004380	chr1:242543171-242543172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532248798	chr1:242543210-242543211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140846771	chr1:242543223-242543224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373608523	chr1:242543248-242543249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10926709	chr1:242543257-242543258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs201836475	chr1:242543306-242543307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537969726	chr1:242543334-242543335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554609162	chr1:242543335-242543336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369302439	chr1:242543344-242543345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10926710	chr1:242543387-242543388	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs184481716	chr1:242543396-242543397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554212314	chr1:242543412-242543413	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs12184245	chr1:242543514-242543515	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368870582	chr1:242543566-242543567	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546134500	chr1:242543568-242543569	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs57647669	chr1:242543625-242543626	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182396195	chr1:242543626-242543627	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242485600-242555400	Weak transcription	Aorta	Aorta
2	chr1:242522600-242555000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:242538000-242555400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:242538600-242549600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:242547000-242547400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:242547200-242548400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:242547200-242575200	Weak transcription	HMEC	breast
8	chr1:242547400-242548000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr1:242547400-242548000	Enhancers	Fetal Brain Male	brain
10	chr1:242547400-242548200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr1:242547400-242555000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:242549600-242549800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:242549800-242580800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:242553800-242555400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:242555000-242555400	Weak transcription	NHEK	skin
16	chr1:242555000-242556200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:242555000-242556200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:242555400-242556000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:242555400-242556000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:242555400-242556000	ZNF genes & repeats	Aorta	Aorta
21	chr1:242555400-242556000	ZNF genes & repeats	NHEK	skin
22	chr1:242555600-242556000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
23	chr1:242555800-242556000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
24	chr1:242556000-242565000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:242556000-242565000	Weak transcription	NHEK	skin
26	chr1:242556000-242575200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:242556000-242586600	Weak transcription	Aorta	Aorta
28	chr1:242556200-242569200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:242556200-242570600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:242561600-242562200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr1:242561800-242566400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:242562000-242562600	Enhancers	Brain Angular Gyrus	brain
33	chr1:242562800-242563200	Enhancers	Fetal Brain Male	brain
34	chr1:242565000-242565400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:242565000-242565400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr1:242565000-242565600	Enhancers	NHEK	skin
37	chr1:242565400-242572800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr1:242565600-242567000	Weak transcription	NHEK	skin
39	chr1:242566400-242566800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:242567800-242569200	Weak transcription	NHEK	skin
41	chr1:242569200-242569600	Enhancers	NHEK	skin
42	chr1:242569200-242569800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:242569800-242575000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:242571800-242572000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:242572000-242574200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:242572800-242573800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:242573200-242575400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr1:242573800-242575000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:242574800-242584800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:242575000-242575800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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