Variant report

Variant	nsv1002445
Chromosome Location	chr1:246112327-246129652
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	chr1:246119639-246119734	K562	blood:	n/a	n/a
2	ATF1	chr1:246119591-246119937	K562	blood:	n/a	n/a
3	ATF1	chr1:246124589-246124813	K562	blood:	n/a	n/a
4	BACH1	chr1:246117937-246117957	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr1:246119570-246119851	K562	blood:	n/a	n/a
6	CEBPB	chr1:246125684-246125791	HepG2	liver:	n/a	chr1:246125707-246125718
7	CHD1	chr1:246117030-246117237	GM12878	blood:	n/a	n/a
8	CHD2	chr1:246116860-246117182	GM12878	blood:	n/a	n/a
9	CTCF	chr1:246124280-246124430	Caco-2	colon:	n/a	n/a
10	CTCF	chr1:246121720-246121870	BE2_C	brain:	n/a	n/a
11	CUX1	chr1:246119671-246119678	K562	blood:	n/a	n/a
12	CUX1	chr1:246115736-246116375	GM12878	blood:	n/a	n/a
13	EBF1	chr1:246115807-246116599	GM12878	blood:	n/a	chr1:246116442-246116453
14	EBF1	chr1:246116880-246117626	GM12878	blood:	n/a	n/a
15	EBF1	chr1:246124213-246124256	GM12878	blood:	n/a	n/a
16	ELF1	chr1:246117712-246117990	GM12878	blood:	n/a	n/a
17	EP300	chr1:246124325-246125600	SK-N-SH	brain:	n/a	chr1:246125373-246125380 chr1:246125529-246125542
18	EP300	chr1:246124535-246124952	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr1:246128813-246128887	GM12878	blood:	n/a	n/a
20	EP300	chr1:246124542-246124875	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr1:246124343-246125156	SK-N-SH	brain:	n/a	n/a
22	EP300	chr1:246116841-246117676	GM12878	blood:	n/a	chr1:246117316-246117330 chr1:246117396-246117404 chr1:246117039-246117049 chr1:246117650-246117664
23	EP300	chr1:246117879-246118012	GM12878	blood:	n/a	n/a
24	EP300	chr1:246119680-246119756	K562	blood:	n/a	n/a
25	FOS	chr1:246119473-246119855	HUVEC	blood vessel:	n/a	chr1:246119623-246119634
26	FOS	chr1:246128715-246128990	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:246123527-246123755	HUVEC	blood vessel:	n/a	n/a
28	FOS	chr1:246128784-246128920	MCF10A-Er-Src	breast:	n/a	n/a
29	FOXA1	chr1:246126955-246127380	HepG2	liver:	n/a	n/a
30	FOXA1	chr1:246117311-246117812	T-47D	breast:	n/a	chr1:246117578-246117593
31	FOXA1	chr1:246126970-246127421	HepG2	liver:	n/a	n/a
32	FOXA1	chr1:246126955-246127269	HepG2	liver:	n/a	n/a
33	FOXA1	chr1:246117432-246117739	T-47D	breast:	n/a	chr1:246117578-246117593
34	FOXA1	chr1:246126969-246127358	HepG2	liver:	n/a	n/a
35	FOXA2	chr1:246126994-246127227	HepG2	liver:	n/a	n/a
36	FOXM1	chr1:246116718-246117972	GM12878	blood:	n/a	n/a
37	GATA2	chr1:246119540-246119916	HUVEC	blood vessel:	n/a	chr1:246119722-246119732 chr1:246119685-246119692
38	GATA3	chr1:246117340-246117856	T-47D	breast:	n/a	n/a
39	GATA3	chr1:246124282-246125106	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr1:246117394-246117470	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr1:246124381-246125070	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr1:246117349-246117810	T-47D	breast:	n/a	n/a
43	HNF4A	chr1:246127025-246127271	HepG2	liver:	n/a	n/a
44	IRF1	chr1:246117121-246117586	K562	blood:	n/a	chr1:246117345-246117356 chr1:246117319-246117332 chr1:246117322-246117333 chr1:246117344-246117358 chr1:246117319-246117332 chr1:246117346-246117357 chr1:246117320-246117337 chr1:246117344-246117361 chr1:246117318-246117332 chr1:246117321-246117332 chr1:246117343-246117356 chr1:246117317-246117331 chr1:246117321-246117331 chr1:246117319-246117332 chr1:246117345-246117359
45	IRF1	chr1:246117320-246117515	K562	blood:	n/a	chr1:246117345-246117356 chr1:246117322-246117333 chr1:246117344-246117358 chr1:246117346-246117357 chr1:246117320-246117337 chr1:246117344-246117361 chr1:246117321-246117332 chr1:246117343-246117356 chr1:246117321-246117331 chr1:246117345-246117359
46	IRF1	chr1:246117041-246117672	K562	blood:	n/a	chr1:246117345-246117356 chr1:246117319-246117332 chr1:246117322-246117333 chr1:246117344-246117358 chr1:246117319-246117332 chr1:246117346-246117357 chr1:246117320-246117337 chr1:246117344-246117361 chr1:246117318-246117332 chr1:246117321-246117332 chr1:246117343-246117356 chr1:246117317-246117331 chr1:246117321-246117331 chr1:246117319-246117332 chr1:246117345-246117359
47	JUND	chr1:246119593-246119837	K562	blood:	n/a	n/a
48	MAX	chr1:246117702-246117861	GM12878	blood:	n/a	n/a
49	MAX	chr1:246116953-246117224	GM12878	blood:	n/a	n/a
50	MAZ	chr1:246115364-246115728	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246125159-246125209	NHDF-neo	bronchial:	n/a
2	chr1:246125159-246125209	SK-N-SH_RA	brain:	n/a
3	chr1:246125159-246125209	HCPEpiC	choroid plexus:	n/a
4	chr1:246125159-246125209	SK-N-SH	brain:	n/a
5	chr1:246125159-246125209	Hepatocyte	liver:	n/a
6	chr1:246125159-246125209	HMEC	breast:	n/a
7	chr1:246125159-246125209	PANC-1	pancreas:	n/a
8	chr1:246125159-246125209	HCT-116	colon:	n/a
9	chr1:246125159-246125209	K562	blood:	n/a
10	chr1:246125159-246125209	GM06990	blood:	n/a
11	chr1:246125159-246125209	A549	lung:	n/a
12	chr1:246125159-246125209	HL-60	blood:	n/a
13	chr1:246125159-246125209	AG09309	skin:	n/a
14	chr1:246125159-246125209	ECC-1	luminal epithelium:	n/a
15	chr1:246125159-246125209	HNPCEpiC	eye:	n/a
16	chr1:246125159-246125209	AG04450	lung:	fetal
17	chr1:246125159-246125209	GM12892	blood:	n/a
18	chr1:246125159-246125209	ProgFib	skin:	n/a
19	chr1:246125159-246125209	HUVEC	blood vessel:	n/a
20	chr1:246125159-246125209	U87	brain:	n/a
21	chr1:246125159-246125209	T-47D	breast:	n/a
22	chr1:246125159-246125209	IMR90	lung:	fetal
23	chr1:246125159-246125209	HCM	heart:	n/a
24	chr1:246125159-246125209	LNCaP	prostate:	n/a
25	chr1:246125159-246125209	GM12891	blood:	n/a
26	chr1:246125159-246125209	HEEpiC	esophagus:	n/a
27	chr1:246125159-246125209	HRCEpiC	kidney:	n/a
28	chr1:246125159-246125209	GM12878	blood:	n/a
29	chr1:246125159-246125209	NB4	blood:	n/a
30	chr1:246125159-246125209	HRPEpiC	eye:	n/a
31	chr1:246125159-246125209	H1-hESC	embryonic stem cell:	embryo
32	chr1:246125159-246125209	ovcar-3	ovarian:	n/a
33	chr1:246125159-246125209	HCF	heart:	n/a
34	chr1:246125159-246125209	NHBE	bronchial:	n/a
35	chr1:246125159-246125209	Jurkat	blood:	n/a
36	chr1:246125159-246125209	CMK	blood:	n/a
37	chr1:246125159-246125209	BJ	skin:	n/a
38	chr1:246125159-246125209	RPTEC	kidney:	n/a
39	chr1:246125159-246125209	Hela-S3	cervix:	n/a
40	chr1:246125159-246125209	PFSK-1	brain:	n/a
41	chr1:246125159-246125209	HEK293	kidney:	embryo
42	chr1:246125159-246125209	SKMC	muscle:	n/a
43	chr1:246125159-246125209	Caco-2	colon:	n/a
44	chr1:246125159-246125209	SK-N-MC	brain:	n/a
45	chr1:246125159-246125209	HepG2	liver:	n/a
46	chr1:246125159-246125209	GM19239	blood:	n/a
47	chr1:246125159-246125209	HAEpiC	amniotic membrane:	n/a
48	chr1:246125159-246125209	PrEC	prostate:	n/a
49	chr1:246125159-246125209	NH-A	brain:	n/a
50	chr1:246125159-246125209	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:246118130..246122848-chr1:246123381..246128902,9	K562	blood:
2	chr1:246114942..246117508-chr1:246123579..246126563,3	K562	blood:
3	chr1:246129359..246131604-chr1:246142419..246144141,2	K562	blood:
4	chr1:246127855..246130595-chr1:246132443..246134267,2	K562	blood:
5	chr1:246115508..246118574-chr1:246120452..246123477,3	K562	blood:
6	chr1:246113571..246115154-chr1:246143779..246145681,2	K562	blood:
7	chr1:246126390..246128678-chr1:246132301..246134356,2	K562	blood:
8	chr1:246109012..246112867-chr1:246113941..246115996,3	K562	blood:
9	chr1:246125821..246128202-chr1:246128524..246131405,2	K562	blood:
10	chr1:246122598..246124565-chr1:246135159..246137741,2	K562	blood:
11	chr1:246115282..246117268-chr20:9203309..9206054,2	MCF-7	breast:
12	chr1:246125821..246128202-chr1:246128524..246131405,2	K562	blood:
13	chr1:246109012..246111892-chr1:246114019..246115996,2	K562	blood:
14	chr1:246114942..246117508-chr1:246123579..246126563,3	K562	blood:
15	chr1:246129149..246130792-chr1:246136104..246138621,2	K562	blood:
16	chr1:246109012..246112867-chr1:246113941..246115996,3	K562	blood:
17	chr1:246115508..246118574-chr1:246120452..246123477,3	K562	blood:

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3	CpG island
ENSG00000185420	chromatin interactions

Extended variants
information (count: 792 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:792 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568064269	chr1:246112350-246112351	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs192568710	chr1:246112353-246112354	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs375852150	chr1:246112364-246112365	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs554642691	chr1:246112387-246112388	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs574808156	chr1:246112436-246112437	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556910888	chr1:246112460-246112461	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554262837	chr1:246112480-246112481	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577426880	chr1:246112512-246112513	Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372087918	chr1:246112607-246112608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375049466	chr1:246112617-246112618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544401947	chr1:246112623-246112624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546013724	chr1:246112624-246112625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562722281	chr1:246112645-246112646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576236086	chr1:246112648-246112649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113810845	chr1:246112654-246112655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150182648	chr1:246112699-246112700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527253768	chr1:246112710-246112711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72768783	chr1:246112734-246112735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73130315	chr1:246112768-246112769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs532901862	chr1:246112796-246112797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189067101	chr1:246112803-246112804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12736658	chr1:246112828-246112829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538139931	chr1:246112833-246112834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548828263	chr1:246112849-246112850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568680557	chr1:246112902-246112903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112939056	chr1:246112971-246112972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139053715	chr1:246112983-246112984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577413214	chr1:246113064-246113065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539967527	chr1:246113085-246113086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538555005	chr1:246113111-246113112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376505931	chr1:246113127-246113128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs55798060	chr1:246113129-246113130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12409712	chr1:246113130-246113131	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs397824412	chr1:246113135-246113136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576153716	chr1:246113137-246113138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528438702	chr1:246113157-246113158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113433124	chr1:246113189-246113190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12091983	chr1:246113198-246113199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs12081763	chr1:246113208-246113209	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs116510451	chr1:246113263-246113264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143288200	chr1:246113276-246113277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112343836	chr1:246113289-246113290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147122060	chr1:246113343-246113344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189385159	chr1:246113355-246113356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531904061	chr1:246113375-246113376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60555554	chr1:246113400-246113401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548508819	chr1:246113405-246113406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370162637	chr1:246113428-246113429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568728588	chr1:246113498-246113499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372276975	chr1:246113503-246113504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Multiple myeloma	16616336	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
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246092800-246116600	Weak transcription	Osteobl	bone
2	chr1:246095000-246113200	Weak transcription	K562	blood
3	chr1:246103800-246115800	Weak transcription	Spleen	Spleen
4	chr1:246103800-246132600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:246109000-246116000	Weak transcription	Primary T cells from cord blood	blood
6	chr1:246109400-246112400	Enhancers	Fetal Stomach	stomach
7	chr1:246110600-246114400	Weak transcription	Right Atrium	heart
8	chr1:246110600-246116600	Weak transcription	Adipose Nuclei	Adipose
9	chr1:246110800-246113600	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr1:246110800-246116600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr1:246110800-246116800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:246110800-246117000	Weak transcription	NHDF-Ad	bronchial
13	chr1:246111000-246113600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:246111000-246115800	Weak transcription	Fetal Brain Male	brain
15	chr1:246111000-246116800	Weak transcription	Fetal Muscle Leg	muscle
16	chr1:246111000-246117000	Weak transcription	Fetal Kidney	kidney
17	chr1:246111400-246112600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:246111600-246112600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:246112000-246112400	Enhancers	Lung	lung
20	chr1:246112000-246112600	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:246112000-246112600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:246112000-246112600	Enhancers	Pancreas	Pancrea
23	chr1:246112200-246112400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr1:246112400-246117000	Weak transcription	Fetal Stomach	stomach
25	chr1:246112400-246117400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:246112400-246117600	Weak transcription	Lung	lung
27	chr1:246112600-246116800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:246112600-246117600	Weak transcription	Pancreas	Pancrea
29	chr1:246112600-246117800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:246112600-246127400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:246112600-246132000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:246112800-246116600	Weak transcription	Primary B cells from cord blood	blood
33	chr1:246113200-246116000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr1:246113200-246116600	Strong transcription	K562	blood
35	chr1:246113600-246114000	Enhancers	Fetal Thymus	thymus
36	chr1:246113600-246114200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr1:246113600-246114600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr1:246114000-246116600	Weak transcription	Fetal Thymus	thymus
39	chr1:246114200-246116800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr1:246114600-246117000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr1:246115000-246115600	Enhancers	GM12878-XiMat	blood
42	chr1:246115600-246117200	Flanking Active TSS	GM12878-XiMat	blood
43	chr1:246115800-246116000	Enhancers	Fetal Brain Male	brain
44	chr1:246115800-246116200	Enhancers	Spleen	Spleen
45	chr1:246115800-246116600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr1:246115800-246116800	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr1:246115800-246116800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr1:246115800-246117000	Enhancers	Primary B cells from peripheral blood	blood
49	chr1:246116000-246116200	Enhancers	Psoas Muscle	Psoas
50	chr1:246116000-246116400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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