Variant report

Variant	nsv468127
Chromosome Location	chr1:216054086-216066437
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	CEBPB	chr1:216060490-216060784	IMR90	lung:	n/a	chr1:216060625-216060636
2	CEBPB	chr1:216055463-216055772	HepG2	liver:	n/a	chr1:216055602-216055615 chr1:216055602-216055615 chr1:216055604-216055615 chr1:216055604-216055615 chr1:216055602-216055613 chr1:216055602-216055615
3	CEBPB	chr1:216055413-216055738	MCF-7	breast:	n/a	chr1:216055602-216055615 chr1:216055602-216055615 chr1:216055604-216055615 chr1:216055604-216055615 chr1:216055602-216055613 chr1:216055602-216055615
4	CEBPB	chr1:216065111-216065415	IMR90	lung:	n/a	n/a
5	CEBPB	chr1:216060514-216060741	HepG2	liver:	n/a	chr1:216060625-216060636
6	CTCF	chr1:216061580-216061730	A549	lung:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
7	CTCF	chr1:216061520-216061770	GM12871	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
8	CTCF	chr1:216061060-216061210	RPTEC	kidney:	n/a	n/a
9	CTCF	chr1:216061200-216061350	HPAF	blood vessel:	n/a	n/a
10	CTCF	chr1:216061640-216061790	HepG2	liver:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
11	CTCF	chr1:216061660-216061810	HFF	foreskin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
12	CTCF	chr1:216061451-216061915	MCF-7	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
13	CTCF	chr1:216061584-216061809	LNCaP	prostate:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
14	CTCF	chr1:216061623-216061747	LNCaP	prostate:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
15	CTCF	chr1:216061684-216061851	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:216061600-216061750	GM12864	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
17	CTCF	chr1:216061754-216061844	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:216061600-216061750	HA-sp	spinal cord:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
19	CTCF	chr1:216061620-216061770	AG04449	skin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
20	CTCF	chr1:216061492-216061904	GM12878	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
21	CTCF	chr1:216061820-216061970	HMEC	breast:	n/a	n/a
22	CTCF	chr1:216061629-216061758	Medullo	brain:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
23	CTCF	chr1:216061610-216061758	K562	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
24	CTCF	chr1:216061420-216061570	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr1:216061598-216061779	GM12878	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
26	CTCF	chr1:216061540-216061690	HCT-116	colon:	n/a	n/a
27	CTCF	chr1:216061667-216061755	NHEK	skin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
28	CTCF	chr1:216061628-216061703	SK-N-SH_RA	brain:	n/a	chr1:216061681-216061699
29	CTCF	chr1:216061540-216061690	GM12869	blood:	n/a	n/a
30	CTCF	chr1:216061566-216061759	HepG2	liver:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
31	CTCF	chr1:216060880-216061030	HPF	lung:	n/a	chr1:216060989-216060996 chr1:216060977-216060998
32	CTCF	chr1:216061620-216061770	BE2_C	brain:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
33	CTCF	chr1:216061600-216061750	HAc	cerebellar:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
34	CTCF	chr1:216061540-216061690	AG09319	gingival:	n/a	n/a
35	CTCF	chr1:216061600-216061750	GM12865	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
36	CTCF	chr1:216061600-216061750	HRPEpiC	eye:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
37	CTCF	chr1:216061619-216061786	ProgFib	skin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
38	CTCF	chr1:216061580-216061730	NB4	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
39	CTCF	chr1:216061460-216061610	NHEK	skin:	n/a	n/a
40	CTCF	chr1:216061640-216061790	WERI-Rb-1	eye:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
41	CTCF	chr1:216061420-216061570	GM12865	blood:	n/a	n/a
42	CTCF	chr1:216061632-216061724	GM10248	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
43	CTCF	chr1:216061443-216061984	MCF-7	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
44	CTCF	chr1:216065141-216065177	Gliobla	brain:	n/a	n/a
45	CTCF	chr1:216061571-216061868	MCF-7	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
46	CTCF	chr1:216064960-216065110	HMF	breast:	n/a	n/a
47	CTCF	chr1:216061618-216061751	Hela-S3	cervix:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
48	CTCF	chr1:216061614-216061720	GM13977	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
49	CTCF	chr1:216061600-216061750	HMEC	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
50	CTCF	chr1:216061711-216061717	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:216058191-216058241	HRCEpiC	kidney:	n/a
2	chr1:216058191-216058241	AG04449	skin:	fetal
3	chr1:216058191-216058241	AoSMC	blood vessel:	n/a
4	chr1:216058191-216058241	GM19239	blood:	n/a
5	chr1:216058191-216058241	GM12892	blood:	n/a
6	chr1:216058191-216058241	Hepatocyte	liver:	n/a
7	chr1:216058191-216058241	SK-N-SH_RA	brain:	n/a
8	chr1:216058191-216058241	ProgFib	skin:	n/a
9	chr1:216058191-216058241	ECC-1	luminal epithelium:	n/a
10	chr1:216058191-216058241	Jurkat	blood:	n/a
11	chr1:216058191-216058241	U87	brain:	n/a
12	chr1:216058191-216058241	Caco-2	colon:	n/a
13	chr1:216058191-216058241	HepG2	liver:	n/a
14	chr1:216058191-216058241	HCT-116	colon:	n/a
15	chr1:216058191-216058241	GM06990	blood:	n/a
16	chr1:216058191-216058241	MCF10A-Er-Src	breast:	n/a
17	chr1:216058191-216058241	NHDF-neo	bronchial:	n/a
18	chr1:216058191-216058241	HNPCEpiC	eye:	n/a
19	chr1:216058191-216058241	NHBE	bronchial:	n/a
20	chr1:216058191-216058241	A549	lung:	n/a
21	chr1:216058191-216058241	T-47D	breast:	n/a
22	chr1:216058191-216058241	HUVEC	blood vessel:	n/a
23	chr1:216058191-216058241	HEK293	kidney:	embryo
24	chr1:216058191-216058241	SKMC	muscle:	n/a
25	chr1:216058191-216058241	AG04450	lung:	fetal
26	chr1:216058191-216058241	BJ	skin:	n/a
27	chr1:216058191-216058241	AG09309	skin:	n/a
28	chr1:216058191-216058241	NB4	blood:	n/a
29	chr1:216058191-216058241	H1-hESC	embryonic stem cell:	embryo
30	chr1:216058191-216058241	GM12878	blood:	n/a
31	chr1:216058191-216058241	HIPEpiC	eye:	n/a
32	chr1:216058191-216058241	Hela-S3	cervix:	n/a
33	chr1:216058191-216058241	RPTEC	kidney:	n/a
34	chr1:216058191-216058241	BE2_C	brain:	n/a
35	chr1:216058191-216058241	SAEC	small airway:	n/a
36	chr1:216058191-216058241	HRPEpiC	eye:	n/a
37	chr1:216058191-216058241	HMEC	breast:	n/a
38	chr1:216058191-216058241	MCF-7	breast:	n/a
39	chr1:216058191-216058241	SK-N-SH	brain:	n/a
40	chr1:216058191-216058241	ovcar-3	ovarian:	n/a
41	chr1:216058191-216058241	AG10803	skin:	n/a
42	chr1:216058191-216058241	HEEpiC	esophagus:	n/a
43	chr1:216058191-216058241	HL-60	blood:	n/a
44	chr1:216058191-216058241	IMR90	lung:	fetal
45	chr1:216058191-216058241	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:216058191-216058241	PrEC	prostate:	n/a
47	chr1:216058191-216058241	PANC-1	pancreas:	n/a
48	chr1:216058191-216058241	K562	blood:	n/a
49	chr1:216058191-216058241	CMK	blood:	n/a
50	chr1:216058191-216058241	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:216061210..216062115-chr1:216367528..216368046,2	MCF-7	breast:
2	chr1:216061208..216061956-chr1:216293049..216293584,2	MCF-7	breast:
3	chr1:215883862..215884424-chr1:216061346..216062151,2	MCF-7	breast:
4	chr1:216061603..216062225-chr1:216207802..216208490,2	MCF-7	breast:
5	chr1:216061653..216062167-chr1:216394272..216395211,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCTD3-1	chr1:216059924-216059983	ENSG00000229242.1

Variant related genes	Relation type
ENSG00000229242	TF binding region
ENSG00000229242	CpG island

Extended variants
information (count: 483 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115796643	chr1:216055202-216055203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143654760	chr1:216055212-216055213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73090764	chr1:216055214-216055215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527567514	chr1:216055215-216055216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7516705	chr1:216055286-216055287	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs552376529	chr1:216055287-216055288	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs569379842	chr1:216055348-216055349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192024495	chr1:216055356-216055357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548572280	chr1:216055372-216055373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568315716	chr1:216055379-216055380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138163798	chr1:216055399-216055400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs67200864	chr1:216055446-216055447	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs554010560	chr1:216055451-216055452	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs142623270	chr1:216055465-216055466	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs12136954	chr1:216055493-216055494	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs556480060	chr1:216055507-216055508	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs575341305	chr1:216055544-216055545	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs543933462	chr1:216055561-216055562	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554554499	chr1:216055589-216055590	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs574449023	chr1:216055646-216055647	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs116651502	chr1:216055666-216055667	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs542942402	chr1:216055671-216055672	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs546992131	chr1:216055694-216055695	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs77398953	chr1:216055696-216055697	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546060748	chr1:216055704-216055705	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs61828253	chr1:216055711-216055712	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs66780075	chr1:216055742-216055743	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182765316	chr1:216055743-216055744	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs139619258	chr1:216055773-216055774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201984046	chr1:216055774-216055775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17567651	chr1:216055853-216055854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534531438	chr1:216055860-216055861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146000632	chr1:216055874-216055875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138648651	chr1:216055894-216055895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547364969	chr1:216055919-216055920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542523478	chr1:216055983-216055984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539738404	chr1:216055993-216055994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs57823793	chr1:216056048-216056049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570694497	chr1:216056060-216056061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1981229	chr1:216056071-216056072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140145656	chr1:216056147-216056148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200743116	chr1:216056148-216056149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560740454	chr1:216056181-216056182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537960233	chr1:216056203-216056204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1981228	chr1:216056210-216056211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113403262	chr1:216056217-216056218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540274753	chr1:216056287-216056288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34744699	chr1:216056318-216056319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553793221	chr1:216056345-216056346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs17025548	chr1:216056348-216056349	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease

Variant related diseases (count:91)

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
Ovarian cancer	21720365	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
Breast cancer	22522925	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216055200-216055400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:216055400-216064200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:216059000-216059600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr1:216059600-216060800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:216060800-216061600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr1:216060800-216062000	Enhancers	Liver	Liver
7	chr1:216061000-216061400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:216061000-216061400	Enhancers	Brain Germinal Matrix	brain
9	chr1:216061000-216061800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr1:216061400-216061600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:216061400-216064200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:216061600-216062800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:216061600-216065000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr1:216062800-216063800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:216063200-216063400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:216063200-216063800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:216063400-216064400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:216063600-216064200	Active TSS	GM12878-XiMat	blood
19	chr1:216063800-216064200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:216063800-216064800	Enhancers	Adipose Nuclei	Adipose
21	chr1:216063800-216065600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:216064200-216064400	Weak transcription	GM12878-XiMat	blood
23	chr1:216064200-216064800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:216064200-216064800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:216064200-216065600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:216064400-216064800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:216064400-216064800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:216064400-216064800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:216064400-216065000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:216064400-216065200	Enhancers	GM12878-XiMat	blood
31	chr1:216064400-216065400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:216064600-216064800	Enhancers	Fetal Kidney	kidney
33	chr1:216064600-216065000	Enhancers	Osteobl	bone
34	chr1:216064600-216065200	Enhancers	NHDF-Ad	bronchial
35	chr1:216064600-216065400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:216064600-216065600	Enhancers	NHLF	lung
37	chr1:216064800-216065000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:216064800-216067600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:216065000-216065200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:216065000-216065200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:216065000-216065200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr1:216065000-216065400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr1:216065000-216065400	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr1:216065200-216065400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr1:216065200-216065400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:216065200-216065400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
47	chr1:216065400-216065800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr1:216065400-216068800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr1:216065600-216066200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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