Variant report

Variant	esv2753128
Chromosome Location	chr1:102843599-103206371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:880)
CpG islands
(count:123)
Chromatin interactive
region (count:14)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:102885486-102885777	HepG2	liver:	n/a	n/a
2	ATF1	chr1:103120954-103121154	K562	blood:	n/a	n/a
3	ATF2	chr1:102963368-102963672	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:102896928-102897159	GM12878	blood:	n/a	chr1:102897077-102897088
5	BCL11A	chr1:102963370-102963761	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr1:102900063-102900391	K562	blood:	n/a	n/a
7	CBX3	chr1:102963353-102963585	K562	blood:	n/a	n/a
8	CBX3	chr1:102900059-102900338	K562	blood:	n/a	n/a
9	CEBPB	chr1:103074238-103074471	HepG2	liver:	n/a	chr1:103074364-103074377 chr1:103074366-103074377 chr1:103074364-103074375
10	CEBPB	chr1:102963413-102963763	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:103054147-103054444	MCF-7	breast:	n/a	n/a
12	CEBPB	chr1:103117704-103117920	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:102845346-102845634	HepG2	liver:	n/a	chr1:102845619-102845632 chr1:102845492-102845503
14	CEBPB	chr1:103142592-103142792	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:103177876-103178058	A549	lung:	n/a	chr1:103177987-103177998
16	CEBPB	chr1:103121175-103121361	K562	blood:	n/a	n/a
17	CEBPB	chr1:102925758-102926021	HepG2	liver:	n/a	chr1:102925877-102925888
18	CEBPB	chr1:102976355-102976559	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:103170856-103171057	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:103177895-103178114	HepG2	liver:	n/a	chr1:103177987-103177998
21	CEBPB	chr1:102843548-102843788	IMR90	lung:	n/a	n/a
22	CHD2	chr1:102900092-102900317	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:102900180-102900330	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr1:103016440-103016590	BE2_C	brain:	n/a	n/a
25	CTCF	chr1:103031840-103031990	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr1:103016400-103016550	K562	blood:	n/a	n/a
27	CTCF	chr1:103016460-103016610	HEK293	kidney:	n/a	n/a
28	CTCF	chr1:103095244-103095409	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:103016500-103016650	GM12866	blood:	n/a	n/a
30	CTCF	chr1:102900180-102900330	HCFaa	heart:	n/a	n/a
31	CTCF	chr1:102900180-102900330	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr1:102900119-102900307	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:102900080-102900230	BE2_C	brain:	n/a	n/a
34	CTCF	chr1:103016460-103016610	HL-60	blood:	n/a	n/a
35	CTCF	chr1:103016480-103016630	HAc	cerebellar:	n/a	n/a
36	CTCF	chr1:103016140-103016889	SK-N-SH	brain:	n/a	n/a
37	CTCF	chr1:102900140-102900290	GM12874	blood:	n/a	n/a
38	CTCF	chr1:103094020-103094170	HMEC	breast:	n/a	n/a
39	CTCF	chr1:103169820-103169853	Lung_OC	lung:	n/a	n/a
40	CTCF	chr1:103016320-103016649	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:103016440-103016590	GM12868	blood:	n/a	n/a
42	CTCF	chr1:103016425-103016617	GM19239	blood:	n/a	n/a
43	CTCF	chr1:102900094-102900346	IMR90	lung:	n/a	n/a
44	CTCF	chr1:103016480-103016630	GM06990	blood:	n/a	n/a
45	CTCF	chr1:102900240-102900390	HMEC	breast:	n/a	n/a
46	CTCF	chr1:102900107-102900354	HepG2	liver:	n/a	n/a
47	CTCF	chr1:102921520-102921670	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:102900120-102900270	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr1:102900139-102900337	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr1:103016455-103016590	NHEK	skin:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:103125518-103125568	HCM	heart:	n/a
2	chr1:103125518-103125568	HCM	heart:	n/a
3	chr1:103125518-103125568	NB4	blood:	n/a
4	chr1:103125518-103125568	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:103125518-103125568	HRPEpiC	eye:	n/a
6	chr1:103125860-103125910	Jurkat	blood:	n/a
7	chr1:103125860-103125910	HCT-116	colon:	n/a
8	chr1:103125518-103125568	HepG2	liver:	n/a
9	chr1:103125860-103125910	SAEC	small airway:	n/a
10	chr1:103125860-103125910	HCF	heart:	n/a
11	chr1:103125860-103125910	HIPEpiC	eye:	n/a
12	chr1:103125518-103125568	HRE	kidney:	n/a
13	chr1:103125518-103125568	SK-N-MC	brain:	n/a
14	chr1:103125518-103125568	ProgFib	skin:	n/a
15	chr1:103125518-103125568	SK-N-SH_RA	brain:	n/a
16	chr1:103125518-103125568	SK-N-SH	brain:	n/a
17	chr1:103125860-103125910	GM12878	blood:	n/a
18	chr1:103125860-103125910	PANC-1	pancreas:	n/a
19	chr1:103125860-103125910	HNPCEpiC	eye:	n/a
20	chr1:103125518-103125568	GM12891	blood:	n/a
21	chr1:103125518-103125568	Jurkat	blood:	n/a
22	chr1:103125860-103125910	SKMC	muscle:	n/a
23	chr1:103125518-103125568	AG09319	gingival:	n/a
24	chr1:103125860-103125910	NHDF-neo	bronchial:	n/a
25	chr1:103125518-103125568	HCF	heart:	n/a
26	chr1:103125860-103125910	H1-hESC	embryonic stem cell:	embryo
27	chr1:103125860-103125910	BE2_C	brain:	n/a
28	chr1:103125860-103125910	GM12891	blood:	n/a
29	chr1:103125860-103125910	HEK293	kidney:	embryo
30	chr1:103125518-103125568	Hela-S3	cervix:	n/a
31	chr1:103125860-103125910	AG04450	lung:	fetal
32	chr1:103125860-103125910	AG09319	gingival:	n/a
33	chr1:103125860-103125910	MCF-7	breast:	n/a
34	chr1:103125860-103125910	A549	lung:	n/a
35	chr1:103125518-103125568	BE2_C	brain:	n/a
36	chr1:103125860-103125910	NHBE	bronchial:	n/a
37	chr1:103125860-103125910	PFSK-1	brain:	n/a
38	chr1:103125860-103125910	GM06990	blood:	n/a
39	chr1:103125518-103125568	HCPEpiC	choroid plexus:	n/a
40	chr1:103125860-103125910	Hela-S3	cervix:	n/a
41	chr1:103125860-103125910	MCF10A-Er-Src	breast:	n/a
42	chr1:103125518-103125568	HNPCEpiC	eye:	n/a
43	chr1:103125518-103125568	HMEC	breast:	n/a
44	chr1:103125860-103125910	K562	blood:	n/a
45	chr1:103125518-103125568	T-47D	breast:	n/a
46	chr1:103125518-103125568	A549	lung:	n/a
47	chr1:103125518-103125568	NH-A	brain:	n/a
48	chr1:103125518-103125568	PFSK-1	brain:	n/a
49	chr1:103125518-103125568	AG10803	skin:	n/a
50	chr1:103125860-103125910	HUVEC	blood vessel:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:103016225..103017019-chr1:103436153..103436688,2	MCF-7	breast:
2	chr1:103125383..103127763-chr1:103133909..103135620,2	K562	blood:
3	chr1:102863880..102865440-chr1:102870522..102872481,2	K562	blood:
4	chr1:102863880..102865440-chr1:102870522..102872481,2	K562	blood:
5	chr1:103059920..103062642-chr1:103088003..103089802,2	MCF-7	breast:
6	chr1:103072742..103074476-chr1:103089450..103092121,2	MCF-7	breast:
7	chr1:103072742..103074476-chr1:103089450..103092121,2	MCF-7	breast:
8	chr1:103059920..103062642-chr1:103088003..103089802,2	MCF-7	breast:
9	chr1:103189403..103191719-chr1:103196207..103198295,2	MCF-7	breast:
10	chr1:103125383..103127763-chr1:103133909..103135620,2	K562	blood:
11	chr1:103150135..103151670-chr1:103153167..103154816,2	K562	blood:
12	chr1:103150135..103151670-chr1:103153167..103154816,2	K562	blood:
13	chr1:103012153..103012701-chr5:175156658..175157566,2	MCF-7	breast:
14	chr1:103189403..103191719-chr1:103196207..103198295,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM3-1	chr1:102852918-102852977	XLOC_000943
2	lnc-OLFM3-1	chr1:102854091-102854185	XLOC_000943
3	lnc-OLFM3-1	chr1:102852644-102852807	XLOC_000943
4	lnc-OLFM3-1	chr1:102854091-102854120	XLOC_000943
5	lnc-COL11A1-3	chr1:103001466-103001649	NONHSAT004876
6	lnc-OLFM3-1	chr1:102852918-102852977	XLOC_000943
7	lnc-OLFM3-1	chr1:102855050-102855163	XLOC_000943
8	lnc-OLFM3-1	chr1:102855050-102855186	XLOC_000943
9	lnc-OLFM3-1	chr1:102853515-102853765	XLOC_000943
10	lnc-RNPC3-3	chr1:103143040-103143147	XLOC_000322
11	lnc-RNPC3-3	chr1:103145340-103145365	XLOC_000322
12	lnc-COL11A1-3	chr1:103011102-103011236	NONHSAT004876
13	lnc-OLFM3-1	chr1:102854091-102854185	XLOC_000943
14	lnc-COL11A1-3	chr1:103091736-103091986	NONHSAT004876
15	lnc-COL11A1-3	chr1:103005919-103005946	NONHSAT004876
16	lnc-COL11A1-3	chr1:103037948-103038072	NONHSAT004876
17	lnc-OLFM3-1	chr1:102852761-102852807	XLOC_000943
18	lnc-COL11A1-3	chr1:103004701-103004800	NONHSAT004876
19	lnc-COL11A1-3	chr1:103005667-103005774	NONHSAT004876
20	lnc-RNPC3-3	chr1:103142328-103142403	XLOC_000322

No data

Variant related genes	Relation type
ENSG00000233359	TF binding region
ENSG00000233359	CpG island
C10orf26	miRNA target sites
PRNP	miRNA target sites
SYNE2	miRNA target sites
LNX2	miRNA target sites
MPHOSPH9	miRNA target sites
GCET2	miRNA target sites

Extended variants
information (count: 1655 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1655 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565020394	chr1:102845852-102845853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532411263	chr1:102845859-102845860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550558802	chr1:102845865-102845866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141684792	chr1:102845887-102845888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530289136	chr1:102845960-102845961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528558228	chr1:102845964-102845965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548787373	chr1:102846011-102846012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182159327	chr1:102846039-102846040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534375814	chr1:102846049-102846050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368174526	chr1:102846073-102846074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553144809	chr1:102846100-102846101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116086917	chr1:102846106-102846107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79486841	chr1:102846117-102846118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368812953	chr1:102846127-102846128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4142739	chr1:102846133-102846134	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs12119077	chr1:102846144-102846145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs11164492	chr1:102846147-102846148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554824218	chr1:102846168-102846169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78123449	chr1:102846171-102846172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181911678	chr1:102852644-102852645	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs554419361	chr1:102852792-102852793	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs540704987	chr1:102852919-102852920	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs2050825	chr1:102852945-102852946	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs1340403	chr1:102852953-102852954	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs542572669	chr1:102852963-102852964	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs529689626	chr1:102853532-102853533	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs180772511	chr1:102853673-102853674	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs151021848	chr1:102853711-102853712	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs532149925	chr1:102853712-102853713	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs76182768	chr1:102853740-102853741	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs367638764	chr1:102853745-102853746	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs570659165	chr1:102853748-102853749	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs541558375	chr1:102855062-102855063	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs190854603	chr1:102855101-102855102	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs115125776	chr1:102855115-102855116	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs545428680	chr1:102855130-102855131	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs371874743	chr1:102855159-102855160	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs182609848	chr1:102855166-102855167	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs376142453	chr1:102855539-102855540	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199506331	chr1:102855631-102855632	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs386367860	chr1:102855632-102855633	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs386367861	chr1:102855643-102855644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs397695301	chr1:102855645-102855646	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377248644	chr1:102855646-102855647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs188008506	chr1:102855664-102855665	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs4907970	chr1:102856473-102856474	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553254656	chr1:102856524-102856525	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs369381810	chr1:102856532-102856533	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs148594709	chr1:102856541-102856542	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs11164497	chr1:102856552-102856553	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102845800-102846200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:102885600-102886000	Enhancers	Liver	Liver
3	chr1:102885600-102886000	Enhancers	HepG2	liver
4	chr1:102900000-102900400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr1:102901200-102901400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:102901200-102901600	Enhancers	GM12878-XiMat	blood
7	chr1:102901400-102901600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:102907800-102908400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr1:102938600-102939000	Enhancers	Fetal Brain Male	brain
10	chr1:102944600-102945000	Enhancers	Dnd41	blood
11	chr1:102945000-102946000	Weak transcription	Dnd41	blood
12	chr1:102946200-102946400	Enhancers	Dnd41	blood
13	chr1:102954000-102954400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr1:102959800-102962200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:103011200-103012000	Enhancers	Fetal Stomach	stomach
16	chr1:103029000-103029800	Active TSS	Primary B cells from cord blood	blood
17	chr1:103029800-103030000	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr1:103051400-103052000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:103051800-103052200	Enhancers	Dnd41	blood
20	chr1:103051800-103053600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr1:103052000-103052400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:103052400-103053600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:103053600-103054200	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr1:103053600-103054200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:103054200-103054400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr1:103054200-103054400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:103075200-103075600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:103075600-103077600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:103076400-103076800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:103076800-103079800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:103077600-103079600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:103079200-103080000	Enhancers	Adipose Nuclei	Adipose
33	chr1:103079800-103080400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:103086400-103087800	Enhancers	Dnd41	blood
35	chr1:103088000-103088600	Enhancers	Fetal Stomach	stomach
36	chr1:103088200-103088800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:103088600-103090400	Weak transcription	Fetal Stomach	stomach
38	chr1:103088800-103095600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:103090400-103090800	Enhancers	Fetal Stomach	stomach
40	chr1:103090800-103091800	Weak transcription	Fetal Stomach	stomach
41	chr1:103091800-103093600	Enhancers	Fetal Stomach	stomach
42	chr1:103093000-103093600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:103093000-103093600	Enhancers	Fetal Lung	lung
44	chr1:103093400-103093600	Enhancers	Brain Substantia Nigra	brain
45	chr1:103093400-103094000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:103093600-103093800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:103093600-103093800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:103093600-103094000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:103093600-103094000	Active TSS	Fetal Stomach	stomach
50	chr1:103093600-103094000	Active TSS	HSMMtube	muscle

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