Variant report

Variant	nsv873378
Chromosome Location	chr1:242654482-242723236
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	BACH1	chr1:242686703-242687743	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr1:242687442-242687642	K562	blood:	n/a	n/a
3	CEBPB	chr1:242718132-242718180	A549	lung:	n/a	n/a
4	CEBPB	chr1:242689119-242689436	A549	lung:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
5	CEBPB	chr1:242689138-242689362	MCF-7	breast:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
6	CEBPB	chr1:242689182-242689351	HepG2	liver:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
7	CEBPB	chr1:242687508-242687635	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:242689091-242689451	K562	blood:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
9	CEBPB	chr1:242721635-242721826	HepG2	liver:	n/a	chr1:242721724-242721735
10	CEBPB	chr1:242689089-242689463	HepG2	liver:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
11	CEBPB	chr1:242688991-242689520	A549	lung:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
12	CEBPB	chr1:242689089-242689448	H1-hESC	embryonic stem cell:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
13	CEBPB	chr1:242689090-242689456	IMR90	lung:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
14	CEBPB	chr1:242689124-242689425	Hela-S3	cervix:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
15	CEBPB	chr1:242695775-242696035	HepG2	liver:	n/a	chr1:242695864-242695873 chr1:242695862-242695873 chr1:242695863-242695874
16	CEBPB	chr1:242689078-242689439	A549	lung:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
17	CHD2	chr1:242688352-242688527	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr1:242666426-242666626	K562	blood:	n/a	n/a
19	CHD2	chr1:242687408-242687754	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr1:242687480-242687886	A549	lung:	n/a	n/a
21	CREB1	chr1:242688020-242688325	A549	lung:	n/a	n/a
22	CTBP2	chr1:242686247-242687755	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:242671551-242671674	MCF-7	breast:	n/a	n/a
24	CTCF	chr1:242687640-242687790	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr1:242687119-242688045	SK-N-SH	brain:	n/a	chr1:242687988-242688001
26	CTCF	chr1:242687320-242687470	AG04449	skin:	n/a	n/a
27	CTCF	chr1:242687280-242687430	HAc	cerebellar:	n/a	n/a
28	CTCF	chr1:242687600-242687750	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr1:242687390-242687448	Gliobla	brain:	n/a	n/a
30	CTCF	chr1:242687660-242687810	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr1:242687299-242687551	A549	lung:	n/a	n/a
32	CTCF	chr1:242687600-242687750	GM12867	blood:	n/a	n/a
33	CTCF	chr1:242687620-242687770	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr1:242688380-242688530	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr1:242687348-242687482	Medullo	brain:	n/a	n/a
36	CTCF	chr1:242687280-242687430	RPTEC	kidney:	n/a	n/a
37	CTCF	chr1:242687733-242687789	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:242671571-242671668	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:242687620-242687770	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:242687360-242687510	HEK293	kidney:	n/a	n/a
41	CTCF	chr1:242687660-242687810	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr1:242687380-242687530	BE2_C	brain:	n/a	n/a
43	CTCF	chr1:242687580-242687730	GM12866	blood:	n/a	n/a
44	CTCF	chr1:242687620-242687770	NHEK	skin:	n/a	n/a
45	CTCF	chr1:242687697-242687814	GM19239	blood:	n/a	n/a
46	CTCF	chr1:242687352-242687484	Fibrobl	skin:	n/a	n/a
47	CTCF	chr1:242687398-242687455	GM19239	blood:	n/a	n/a
48	CTCF	chr1:242687320-242687470	NHEK	skin:	n/a	n/a
49	CTCF	chr1:242688140-242688290	HMEC	breast:	n/a	n/a
50	CTCF	chr1:242687690-242687802	Fibrobl	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242686709-242686759	HMEC	breast:	n/a
2	chr1:242688681-242688731	Hela-S3	cervix:	n/a
3	chr1:242688081-242688131	SK-N-SH_RA	brain:	n/a
4	chr1:242688144-242688194	HNPCEpiC	eye:	n/a
5	chr1:242683142-242683192	AG10803	skin:	n/a
6	chr1:242687527-242687577	HEK293	kidney:	embryo
7	chr1:242688144-242688194	K562	blood:	n/a
8	chr1:242687412-242687462	GM19239	blood:	n/a
9	chr1:242687527-242687577	SAEC	small airway:	n/a
10	chr1:242687465-242687515	HCF	heart:	n/a
11	chr1:242688226-242688276	U87	brain:	n/a
12	chr1:242688681-242688731	ECC-1	luminal epithelium:	n/a
13	chr1:242684042-242684092	GM06990	blood:	n/a
14	chr1:242687412-242687462	HCT-116	colon:	n/a
15	chr1:242686709-242686759	NT2-D1	testis:	n/a
16	chr1:242690733-242690783	PANC-1	pancreas:	n/a
17	chr1:242683142-242683192	HL-60	blood:	n/a
18	chr1:242688081-242688131	GM12891	blood:	n/a
19	chr1:242684042-242684092	RPTEC	kidney:	n/a
20	chr1:242688144-242688194	HCPEpiC	choroid plexus:	n/a
21	chr1:242688681-242688731	HL-60	blood:	n/a
22	chr1:242688081-242688131	ProgFib	skin:	n/a
23	chr1:242683142-242683192	NT2-D1	testis:	n/a
24	chr1:242687527-242687577	GM12892	blood:	n/a
25	chr1:242688523-242688573	HEEpiC	esophagus:	n/a
26	chr1:242688226-242688276	HAEpiC	amniotic membrane:	n/a
27	chr1:242687018-242687068	HCF	heart:	n/a
28	chr1:242688144-242688194	PFSK-1	brain:	n/a
29	chr1:242688144-242688194	Jurkat	blood:	n/a
30	chr1:242688681-242688731	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:242690593-242690643	SK-N-SH	brain:	n/a
32	chr1:242684042-242684092	HCF	heart:	n/a
33	chr1:242687018-242687068	A549	lung:	n/a
34	chr1:242687465-242687515	NHDF-neo	bronchial:	n/a
35	chr1:242683142-242683192	HIPEpiC	eye:	n/a
36	chr1:242687527-242687577	HMEC	breast:	n/a
37	chr1:242688081-242688131	HCPEpiC	choroid plexus:	n/a
38	chr1:242688081-242688131	PFSK-1	brain:	n/a
39	chr1:242688081-242688131	GM06990	blood:	n/a
40	chr1:242688591-242688641	SK-N-SH	brain:	n/a
41	chr1:242688144-242688194	HRCEpiC	kidney:	n/a
42	chr1:242690733-242690783	ovcar-3	ovarian:	n/a
43	chr1:242687465-242687515	HEEpiC	esophagus:	n/a
44	chr1:242690593-242690643	LNCaP	prostate:	n/a
45	chr1:242688320-242688370	SK-N-SH	brain:	n/a
46	chr1:242690593-242690643	NH-A	brain:	n/a
47	chr1:242688320-242688370	GM19239	blood:	n/a
48	chr1:242683142-242683192	HNPCEpiC	eye:	n/a
49	chr1:242684042-242684092	HNPCEpiC	eye:	n/a
50	chr1:242688523-242688573	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:242690016..242691872-chr1:242693633..242696620,2	K562	blood:
2	chr1:242687782..242688282-chr7:140396130..140396992,2	MCF-7	breast:
3	chr1:242687461..242689938-chr1:242691020..242693615,2	K562	blood:
4	chr1:242680127..242681627-chr2:114917951..114919998,2	K562	blood:
5	chr1:242690016..242691872-chr1:242693633..242696620,2	K562	blood:
6	chr1:242687074..242690257-chr1:242691020..242695095,4	K562	blood:
7	chr1:242692263..242693064-chr17:56708576..56709248,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLD5-1	chr1:242692647-242692740	NONHSAT010569
2	lnc-PLD5-1	chr1:242693049-242693341	NONHSAT010569
3	lnc-MAP1LC3C-5	chr1:242676012-242676332	expReg_chr1_22653_-
4	lnc-PLD5-2	chr1:242717724-242718022	XLOC_001281
5	lnc-MAP1LC3C-6	chr1:242680432-242680918	expReg_chr1_22659_-
6	lnc-MAP1LC3C-4	chr1:242654836-242655140	expReg_chr1_22645_-
7	lnc-PLD5-2	chr1:242717038-242717147	XLOC_001281
8	lnc-MAP1LC3C-3	chr1:242654490-242654577	NONHSAT010568
9	lnc-PLD5-1	chr1:242690923-242691021	NONHSAT010569
10	lnc-MAP1LC3C-7	chr1:242681118-242681325	expReg_chr1_22661_-

Variant related genes	Relation type
PLD5	TF binding region
PLD5	CpG island
ENSG00000212195	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000240889	chromatin interactions
ENSG00000180287	chromatin interactions
DACT1	miRNA target sites
DAB2IP	miRNA target sites

Extended variants
information (count: 2739 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2739 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6429360	chr1:242654482-242654483	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533727339	chr1:242654487-242654488	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73144095	chr1:242654494-242654495	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs150532250	chr1:242654506-242654507	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs565968592	chr1:242654524-242654525	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs535089890	chr1:242654542-242654543	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs571827176	chr1:242654547-242654548	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs111369388	chr1:242654551-242654552	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs552686278	chr1:242654626-242654627	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576587757	chr1:242654662-242654663	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545594618	chr1:242654695-242654696	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542816366	chr1:242654712-242654713	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563327005	chr1:242654718-242654719	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541795483	chr1:242654846-242654847	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs191012034	chr1:242654867-242654868	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs138606723	chr1:242654962-242654963	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs527310915	chr1:242654978-242654979	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs541086702	chr1:242654989-242654990	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs182167955	chr1:242655061-242655062	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs79783470	chr1:242655088-242655089	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs533519986	chr1:242655112-242655113	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs149304001	chr1:242655136-242655137	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs570295709	chr1:242655174-242655175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529589281	chr1:242655182-242655183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549432729	chr1:242655210-242655211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112247476	chr1:242655258-242655259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538536127	chr1:242655299-242655300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6695046	chr1:242655301-242655302	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs551803503	chr1:242655369-242655370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571402178	chr1:242655373-242655374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117385616	chr1:242655393-242655394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139779683	chr1:242655434-242655435	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575864515	chr1:242655461-242655462	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549082098	chr1:242655479-242655480	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187763878	chr1:242655492-242655493	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535714969	chr1:242655508-242655509	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192721843	chr1:242655529-242655530	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571966444	chr1:242655542-242655543	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184591423	chr1:242655580-242655581	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564119206	chr1:242655586-242655587	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188335068	chr1:242655587-242655588	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145273631	chr1:242655611-242655612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192053995	chr1:242655612-242655613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529478426	chr1:242655619-242655620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549609738	chr1:242655657-242655658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113877157	chr1:242655661-242655662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370321024	chr1:242655662-242655663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9919232	chr1:242655679-242655680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559795863	chr1:242655690-242655691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184644090	chr1:242655701-242655702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242641200-242660200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:242641800-242663000	Weak transcription	Aorta	Aorta
3	chr1:242645400-242655400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:242651400-242655000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:242652400-242654600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr1:242652400-242654800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:242653200-242654600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:242653800-242658000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:242654600-242655800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:242655000-242656200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:242655400-242655600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:242655600-242656600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:242655800-242656000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:242656000-242659800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:242656200-242657000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:242656600-242657000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:242656800-242657200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:242657000-242657200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:242657000-242660000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:242657200-242657600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:242657200-242660000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:242657600-242658000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:242657600-242658000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:242658000-242658200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr1:242658000-242660200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:242658200-242658600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:242659200-242659600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr1:242659800-242664200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:242660000-242660400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:242660000-242661200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:242660200-242660400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:242660200-242661000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:242660400-242663000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:242660400-242663200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:242661000-242666400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:242661200-242663000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:242663000-242663400	Enhancers	Esophagus	oesophagus
38	chr1:242663000-242663600	Enhancers	Aorta	Aorta
39	chr1:242663000-242664000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:242663000-242664000	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr1:242663000-242664200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr1:242663000-242664800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:242663200-242663400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:242663400-242664200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:242663400-242670000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:242663600-242670200	Weak transcription	Aorta	Aorta
47	chr1:242664000-242670000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:242664200-242666800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:242664200-242679800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:242664800-242666600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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