Variant report

Variant	nsv535301
Chromosome Location	chr1:221692621-221773945
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	ATF1	chr1:221768533-221768534	K562	blood:	n/a	n/a
2	ATF1	chr1:221728375-221728513	K562	blood:	n/a	n/a
3	ATF1	chr1:221741072-221741272	K562	blood:	n/a	n/a
4	ATF1	chr1:221757163-221757521	K562	blood:	n/a	n/a
5	ATF1	chr1:221738143-221738299	K562	blood:	n/a	n/a
6	ATF1	chr1:221701385-221701508	K562	blood:	n/a	n/a
7	BRCA1	chr1:221728602-221728604	GM12878	blood:	n/a	n/a
8	CEBPB	chr1:221762144-221762471	HepG2	liver:	n/a	chr1:221762296-221762307
9	CEBPB	chr1:221751888-221752022	H1-hESC	embryonic stem cell:	n/a	chr1:221752009-221752020
10	CEBPB	chr1:221741557-221741737	H1-hESC	embryonic stem cell:	n/a	chr1:221741647-221741658
11	CEBPB	chr1:221762172-221762436	A549	lung:	n/a	chr1:221762296-221762307
12	CEBPB	chr1:221741506-221741796	K562	blood:	n/a	chr1:221741647-221741658
13	CEBPB	chr1:221751845-221752131	K562	blood:	n/a	chr1:221752009-221752020
14	CEBPB	chr1:221741481-221741795	HepG2	liver:	n/a	chr1:221741647-221741658
15	CEBPB	chr1:221741473-221741818	Hela-S3	cervix:	n/a	chr1:221741647-221741658
16	CEBPB	chr1:221730322-221730611	HepG2	liver:	n/a	chr1:221730452-221730463 chr1:221730453-221730464
17	CEBPB	chr1:221701576-221701816	IMR90	lung:	n/a	chr1:221701688-221701699
18	CEBPB	chr1:221695971-221696179	IMR90	lung:	n/a	chr1:221696104-221696117 chr1:221696104-221696117 chr1:221696104-221696115
19	CEBPB	chr1:221701536-221701821	Hela-S3	cervix:	n/a	chr1:221701688-221701699
20	CEBPB	chr1:221751861-221752093	HepG2	liver:	n/a	chr1:221752009-221752020
21	CEBPB	chr1:221747023-221747621	MCF-7	breast:	n/a	chr1:221747364-221747375 chr1:221747365-221747376 chr1:221747366-221747375
22	CEBPB	chr1:221762140-221762477	K562	blood:	n/a	chr1:221762296-221762307
23	CEBPB	chr1:221730310-221730633	IMR90	lung:	n/a	chr1:221730452-221730463 chr1:221730453-221730464
24	CEBPB	chr1:221756404-221756499	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:221741216-221741836	A549	lung:	n/a	chr1:221741647-221741658
26	CEBPB	chr1:221703748-221703880	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:221741474-221741829	IMR90	lung:	n/a	chr1:221741647-221741658
28	CEBPB	chr1:221747301-221747412	Hela-S3	cervix:	n/a	chr1:221747364-221747375 chr1:221747365-221747376 chr1:221747366-221747375
29	CEBPB	chr1:221701584-221701842	HepG2	liver:	n/a	chr1:221701688-221701699
30	CEBPB	chr1:221730330-221730562	A549	lung:	n/a	chr1:221730452-221730463 chr1:221730453-221730464
31	CEBPB	chr1:221747205-221747548	IMR90	lung:	n/a	chr1:221747364-221747375 chr1:221747365-221747376 chr1:221747366-221747375
32	CEBPB	chr1:221762131-221762446	IMR90	lung:	n/a	chr1:221762296-221762307
33	CEBPB	chr1:221701591-221701818	A549	lung:	n/a	chr1:221701688-221701699
34	CEBPB	chr1:221699128-221699359	Hela-S3	cervix:	n/a	chr1:221699196-221699209
35	CEBPB	chr1:221747118-221747589	MCF-7	breast:	n/a	chr1:221747364-221747375 chr1:221747365-221747376 chr1:221747366-221747375
36	CEBPB	chr1:221747215-221747553	K562	blood:	n/a	chr1:221747364-221747375 chr1:221747365-221747376 chr1:221747366-221747375
37	CEBPB	chr1:221747193-221747541	HepG2	liver:	n/a	chr1:221747364-221747375 chr1:221747365-221747376 chr1:221747366-221747375
38	CTCF	chr1:221717091-221717317	Gliobla	brain:	n/a	chr1:221717238-221717254 chr1:221717239-221717260
39	CTCF	chr1:221717180-221717330	AG04449	skin:	n/a	chr1:221717238-221717254 chr1:221717239-221717260
40	CTCF	chr1:221717160-221717310	GM12870	blood:	n/a	chr1:221717238-221717254 chr1:221717239-221717260
41	CTCF	chr1:221711940-221712087	Gliobla	brain:	n/a	n/a
42	CTCF	chr1:221717160-221717310	HMEC	breast:	n/a	chr1:221717238-221717254 chr1:221717239-221717260
43	CTCF	chr1:221717015-221717441	GM12878	blood:	n/a	chr1:221717238-221717254 chr1:221717239-221717260
44	CTCF	chr1:221693393-221693407	ProgFib	skin:	n/a	n/a
45	CTCF	chr1:221693320-221693470	BE2_C	brain:	n/a	n/a
46	CTCF	chr1:221719540-221719690	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr1:221717080-221717230	GM12865	blood:	n/a	n/a
48	CTCF	chr1:221716800-221716950	HPF	lung:	n/a	n/a
49	CTCF	chr1:221717100-221717250	AG04450	lung:	n/a	n/a
50	CTCF	chr1:221717120-221717270	GM12864	blood:	n/a	chr1:221717238-221717254 chr1:221717239-221717260

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:221747446-221747496	T-47D	breast:	n/a
2	chr1:221747446-221747496	HepG2	liver:	n/a
3	chr1:221737206-221737256	HNPCEpiC	eye:	n/a
4	chr1:221741553-221741603	GM19239	blood:	n/a
5	chr1:221737206-221737256	HRPEpiC	eye:	n/a
6	chr1:221741553-221741603	ProgFib	skin:	n/a
7	chr1:221741553-221741603	GM12878	blood:	n/a
8	chr1:221737032-221737082	GM19239	blood:	n/a
9	chr1:221747446-221747496	HRPEpiC	eye:	n/a
10	chr1:221741553-221741603	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:221741553-221741603	SKMC	muscle:	n/a
12	chr1:221737032-221737082	A549	lung:	n/a
13	chr1:221747446-221747496	SAEC	small airway:	n/a
14	chr1:221737206-221737256	SKMC	muscle:	n/a
15	chr1:221737206-221737256	HRE	kidney:	n/a
16	chr1:221737206-221737256	HCT-116	colon:	n/a
17	chr1:221737032-221737082	U87	brain:	n/a
18	chr1:221737206-221737256	BJ	skin:	n/a
19	chr1:221737206-221737256	CMK	blood:	n/a
20	chr1:221737206-221737256	ECC-1	luminal epithelium:	n/a
21	chr1:221737206-221737256	BE2_C	brain:	n/a
22	chr1:221741553-221741603	SK-N-MC	brain:	n/a
23	chr1:221747446-221747496	HEK293	kidney:	embryo
24	chr1:221737032-221737082	ProgFib	skin:	n/a
25	chr1:221747446-221747496	HL-60	blood:	n/a
26	chr1:221737206-221737256	HEEpiC	esophagus:	n/a
27	chr1:221737032-221737082	GM12891	blood:	n/a
28	chr1:221747446-221747496	NB4	blood:	n/a
29	chr1:221737032-221737082	CMK	blood:	n/a
30	chr1:221741553-221741603	AG09319	gingival:	n/a
31	chr1:221737032-221737082	Caco-2	colon:	n/a
32	chr1:221741553-221741603	NH-A	brain:	n/a
33	chr1:221741553-221741603	NB4	blood:	n/a
34	chr1:221737032-221737082	AG04449	skin:	fetal
35	chr1:221741553-221741603	T-47D	breast:	n/a
36	chr1:221747446-221747496	NHBE	bronchial:	n/a
37	chr1:221737206-221737256	PrEC	prostate:	n/a
38	chr1:221737032-221737082	MCF-7	breast:	n/a
39	chr1:221737032-221737082	HNPCEpiC	eye:	n/a
40	chr1:221747446-221747496	K562	blood:	n/a
41	chr1:221737206-221737256	AG04450	lung:	fetal
42	chr1:221737032-221737082	GM12892	blood:	n/a
43	chr1:221741553-221741603	PrEC	prostate:	n/a
44	chr1:221737206-221737256	HUVEC	blood vessel:	n/a
45	chr1:221737206-221737256	ProgFib	skin:	n/a
46	chr1:221747446-221747496	U87	brain:	n/a
47	chr1:221747446-221747496	SK-N-MC	brain:	n/a
48	chr1:221737206-221737256	MCF-7	breast:	n/a
49	chr1:221741553-221741603	HCPEpiC	choroid plexus:	n/a
50	chr1:221737032-221737082	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:221725072..221727435-chr1:221733629..221736016,2	K562	blood:
2	chr1:221746709..221748888-chr1:221752322..221754674,2	K562	blood:
3	chr1:221746709..221748888-chr1:221752322..221754674,2	K562	blood:
4	chr1:221716913..221720065-chr1:221720989..221725368,3	K562	blood:
5	chr1:221732770..221734353-chr1:221737338..221739600,2	MCF-7	breast:
6	chr1:221746909..221748850-chr1:221913979..221916326,2	MCF-7	breast:
7	chr1:221696861..221698748-chr1:221709544..221711266,2	K562	blood:
8	chr1:221716979..221717540-chr1:221914806..221915585,2	MCF-7	breast:
9	chr1:221766078..221767726-chr1:221770721..221773346,2	MCF-7	breast:
10	chr1:221766487..221768171-chr1:221768648..221770195,2	MCF-7	breast:
11	chr1:221766487..221768171-chr1:221768648..221770195,2	MCF-7	breast:
12	chr1:221696861..221698748-chr1:221709544..221711266,2	K562	blood:
13	chr1:221766078..221767726-chr1:221770721..221773346,2	MCF-7	breast:
14	chr1:221725072..221727435-chr1:221733629..221736016,2	K562	blood:
15	chr1:221716805..221717802-chr1:221811163..221812344,4	MCF-7	breast:
16	chr1:221732770..221734353-chr1:221737338..221739600,2	MCF-7	breast:
17	chr1:221768064..221770595-chr1:221774994..221777506,2	MCF-7	breast:
18	chr1:221746221..221748385-chr1:221914504..221916703,2	MCF-7	breast:
19	chr1:221716861..221717502-chr1:222278572..222279282,2	MCF-7	breast:
20	chr1:221751248..221753271-chr1:221864470..221866458,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DUSP10-2	chr1:221736650-221736978	XLOC_001212
2	lnc-HLX-5	chr1:221722606-221722817	NONHSAT009642
3	lnc-DUSP10-6	chr1:221723128-221723985	NONHSAT009643
4	lnc-DUSP10-2	chr1:221734408-221734479	XLOC_001212
5	lnc-HLX-5	chr1:221727429-221727771	NONHSAT009642
6	lnc-DUSP10-2	chr1:221728934-221729770	XLOC_001212
7	lnc-DUSP10-2	chr1:221728928-221729770	NONHSAT009644
8	lnc-DUSP10-2	chr1:221734408-221734479	NONHSAT009644
9	lnc-DUSP10-2	chr1:221736650-221736994	NONHSAT009644

Variant related genes	Relation type
ENSG00000227585	TF binding region
ENSG00000227585	CpG island
ENSG00000143507	chromatin interactions
ENSG00000227585	chromatin interactions
RGPD4	miRNA target sites
ARID4A	miRNA target sites
CORO2B	miRNA target sites

Extended variants
information (count: 2126 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2126 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141851844	chr1:221692665-221692666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563544260	chr1:221692666-221692667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530174288	chr1:221692671-221692672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548152489	chr1:221692741-221692742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79609237	chr1:221692758-221692759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537539267	chr1:221692761-221692762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192896650	chr1:221692806-221692807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374091583	chr1:221692861-221692862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185105342	chr1:221692871-221692872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190034375	chr1:221692885-221692886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61553069	chr1:221692893-221692894	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs56205442	chr1:221692911-221692912	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs150622116	chr1:221692913-221692914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112807747	chr1:221692917-221692918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576140156	chr1:221692932-221692933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543494063	chr1:221692958-221692959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142080295	chr1:221692984-221692985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532243869	chr1:221693005-221693006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182259608	chr1:221693009-221693010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17010220	chr1:221693023-221693024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs529917826	chr1:221693098-221693099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548115783	chr1:221693113-221693114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569707857	chr1:221693144-221693145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146331702	chr1:221693179-221693180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185633375	chr1:221693188-221693189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554455710	chr1:221693206-221693207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570814842	chr1:221693284-221693285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535132857	chr1:221693285-221693286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553573618	chr1:221693289-221693290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188057581	chr1:221693342-221693343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536139527	chr1:221693362-221693363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557726335	chr1:221693374-221693375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575987164	chr1:221693396-221693397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530984498	chr1:221693406-221693407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549553430	chr1:221693438-221693439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs180961504	chr1:221693444-221693445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375230214	chr1:221693562-221693563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568146948	chr1:221693614-221693615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74144292	chr1:221693629-221693630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs559108917	chr1:221693658-221693659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185422727	chr1:221693686-221693687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548079055	chr1:221693688-221693689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536936533	chr1:221693698-221693699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557152161	chr1:221693741-221693742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75107344	chr1:221693750-221693751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147474768	chr1:221693771-221693772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143298242	chr1:221693773-221693774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563199113	chr1:221693779-221693780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576938368	chr1:221693802-221693803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149458916	chr1:221693812-221693813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	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
Prostate cancer	18632612	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
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221690800-221694600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:221694600-221696800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:221694800-221695200	Enhancers	HSMM	muscle
4	chr1:221694800-221695800	Enhancers	Primary T cells fromperipheralblood	blood
5	chr1:221695000-221696400	Enhancers	Osteobl	bone
6	chr1:221695200-221695800	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr1:221696000-221696400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:221700600-221701200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr1:221701400-221702200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:221701600-221701800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:221701800-221703400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:221702200-221702800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr1:221702200-221704000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:221703400-221704800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:221704000-221704600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:221704000-221704600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr1:221704000-221704600	Enhancers	NHDF-Ad	bronchial
18	chr1:221704200-221704600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:221713000-221716200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:221714800-221715200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:221716000-221717200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:221716000-221717200	Enhancers	NHEK	skin
23	chr1:221716000-221717400	Enhancers	HMEC	breast
24	chr1:221716200-221716600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:221716200-221717200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr1:221716200-221717400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:221716200-221717600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr1:221716400-221717200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr1:221716400-221717200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr1:221716600-221716800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr1:221716600-221717200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr1:221716600-221717200	Enhancers	H9 Cell Line	embryonic stem cell
33	chr1:221716600-221717400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr1:221716800-221717200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:221716800-221717200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:221716800-221717200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:221716800-221717200	Enhancers	Stomach Smooth Muscle	stomach
38	chr1:221716800-221717400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:221716800-221717600	Enhancers	Liver	Liver
40	chr1:221717000-221717200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:221717000-221717200	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr1:221717000-221717200	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr1:221717000-221717400	Enhancers	Adipose Nuclei	Adipose
44	chr1:221717000-221717400	Enhancers	Brain Anterior Caudate	brain
45	chr1:221717000-221717800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:221717600-221721400	Weak transcription	Liver	Liver
47	chr1:221721400-221724000	Enhancers	Liver	Liver
48	chr1:221722200-221724400	Enhancers	Pancreas	Pancrea
49	chr1:221723000-221724000	Enhancers	HMEC	breast
50	chr1:221723400-221723600	Enhancers	Fetal Heart	heart

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