Variant report

Variant	nsv535004
Chromosome Location	chr1:75716654-75936048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1210)
CpG islands
(count:122)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:75738778-75739068	K562	blood:	n/a	n/a
2	ARID3A	chr1:75888899-75889838	K562	blood:	n/a	n/a
3	ARID3A	chr1:75887891-75888450	K562	blood:	n/a	n/a
4	ARID3A	chr1:75819638-75820397	K562	blood:	n/a	n/a
5	ARID3A	chr1:75878436-75878779	K562	blood:	n/a	n/a
6	ARID3A	chr1:75921956-75921991	K562	blood:	n/a	n/a
7	ARID3A	chr1:75731381-75731886	HepG2	liver:	n/a	n/a
8	ATF1	chr1:75770784-75770860	K562	blood:	n/a	n/a
9	ATF1	chr1:75902808-75902957	K562	blood:	n/a	n/a
10	ATF1	chr1:75738849-75739154	K562	blood:	n/a	n/a
11	ATF1	chr1:75904090-75904413	K562	blood:	n/a	n/a
12	ATF1	chr1:75878326-75878705	K562	blood:	n/a	n/a
13	ATF1	chr1:75889272-75889641	K562	blood:	n/a	n/a
14	ATF1	chr1:75820019-75820285	K562	blood:	n/a	n/a
15	ATF1	chr1:75731435-75731750	K562	blood:	n/a	n/a
16	ATF1	chr1:75796320-75796780	K562	blood:	n/a	n/a
17	ATF2	chr1:75804653-75805344	GM12878	blood:	n/a	n/a
18	ATF2	chr1:75804690-75805392	GM12878	blood:	n/a	n/a
19	ATF3	chr1:75878356-75878660	K562	blood:	n/a	n/a
20	BACH1	chr1:75935646-75935837	K562	blood:	n/a	n/a
21	BACH1	chr1:75802552-75802739	K562	blood:	n/a	n/a
22	BACH1	chr1:75933751-75933871	K562	blood:	n/a	n/a
23	BACH1	chr1:75898472-75898473	K562	blood:	n/a	n/a
24	BACH1	chr1:75860456-75860736	K562	blood:	n/a	chr1:75860631-75860645
25	BATF	chr1:75804735-75805103	GM12878	blood:	n/a	n/a
26	BATF	chr1:75804688-75805234	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:75804766-75805234	GM12878	blood:	n/a	chr1:75804998-75805007 chr1:75805078-75805087 chr1:75805077-75805086
28	BHLHE40	chr1:75731442-75731768	HepG2	liver:	n/a	n/a
29	BHLHE40	chr1:75840049-75840076	K562	blood:	n/a	n/a
30	BHLHE40	chr1:75731403-75731705	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:75839104-75839347	K562	blood:	n/a	n/a
32	BHLHE40	chr1:75889314-75889840	K562	blood:	n/a	n/a
33	BHLHE40	chr1:75905974-75906431	K562	blood:	n/a	n/a
34	BHLHE40	chr1:75794331-75794695	K562	blood:	n/a	n/a
35	BHLHE40	chr1:75804819-75805062	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:75878374-75878636	K562	blood:	n/a	n/a
37	BHLHE40	chr1:75839714-75839746	K562	blood:	n/a	n/a
38	BHLHE40	chr1:75904161-75904195	K562	blood:	n/a	n/a
39	BHLHE40	chr1:75915666-75916013	K562	blood:	n/a	n/a
40	BHLHE40	chr1:75804373-75804610	GM12878	blood:	n/a	n/a
41	CBX3	chr1:75881984-75882261	K562	blood:	n/a	n/a
42	CBX3	chr1:75832317-75832654	K562	blood:	n/a	n/a
43	CBX3	chr1:75880847-75881215	K562	blood:	n/a	n/a
44	CBX3	chr1:75832305-75832631	K562	blood:	n/a	n/a
45	CBX3	chr1:75819901-75820405	K562	blood:	n/a	n/a
46	CBX3	chr1:75881926-75882288	K562	blood:	n/a	n/a
47	CCNT2	chr1:75888912-75889651	K562	blood:	n/a	n/a
48	CCNT2	chr1:75915752-75916067	K562	blood:	n/a	n/a
49	CCNT2	chr1:75819899-75820649	K562	blood:	n/a	n/a
50	CEBPB	chr1:75890727-75891050	H1-hESC	embryonic stem cell:	n/a	chr1:75890876-75890887 chr1:75890875-75890886

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:75841810-75841860	PFSK-1	brain:	n/a
2	chr1:75808730-75808780	CMK	blood:	n/a
3	chr1:75841810-75841860	HAEpiC	amniotic membrane:	n/a
4	chr1:75808730-75808780	HEK293	kidney:	embryo
5	chr1:75841810-75841860	HNPCEpiC	eye:	n/a
6	chr1:75841810-75841860	HRE	kidney:	n/a
7	chr1:75841810-75841860	AG09309	skin:	n/a
8	chr1:75808730-75808780	HUVEC	blood vessel:	n/a
9	chr1:75841810-75841860	A549	lung:	n/a
10	chr1:75841810-75841860	HIPEpiC	eye:	n/a
11	chr1:75841810-75841860	AG04450	lung:	fetal
12	chr1:75841810-75841860	BE2_C	brain:	n/a
13	chr1:75808730-75808780	Hela-S3	cervix:	n/a
14	chr1:75841810-75841860	MCF-7	breast:	n/a
15	chr1:75808730-75808780	ProgFib	skin:	n/a
16	chr1:75808730-75808780	Caco-2	colon:	n/a
17	chr1:75841810-75841860	GM06990	blood:	n/a
18	chr1:75808730-75808780	HIPEpiC	eye:	n/a
19	chr1:75808730-75808780	HAEpiC	amniotic membrane:	n/a
20	chr1:75841810-75841860	HEK293	kidney:	embryo
21	chr1:75808730-75808780	NHBE	bronchial:	n/a
22	chr1:75841810-75841860	Hela-S3	cervix:	n/a
23	chr1:75808730-75808780	H1-hESC	embryonic stem cell:	embryo
24	chr1:75808730-75808780	HL-60	blood:	n/a
25	chr1:75841810-75841860	HCT-116	colon:	n/a
26	chr1:75808730-75808780	NB4	blood:	n/a
27	chr1:75808730-75808780	GM19239	blood:	n/a
28	chr1:75841810-75841860	GM12891	blood:	n/a
29	chr1:75808730-75808780	HCT-116	colon:	n/a
30	chr1:75808730-75808780	SKMC	muscle:	n/a
31	chr1:75808730-75808780	IMR90	lung:	fetal
32	chr1:75841810-75841860	AG10803	skin:	n/a
33	chr1:75841810-75841860	SAEC	small airway:	n/a
34	chr1:75841810-75841860	AoSMC	blood vessel:	n/a
35	chr1:75841810-75841860	SK-N-SH	brain:	n/a
36	chr1:75841810-75841860	K562	blood:	n/a
37	chr1:75808730-75808780	SK-N-SH_RA	brain:	n/a
38	chr1:75841810-75841860	MCF10A-Er-Src	breast:	n/a
39	chr1:75841810-75841860	BJ	skin:	n/a
40	chr1:75808730-75808780	AoSMC	blood vessel:	n/a
41	chr1:75808730-75808780	GM12891	blood:	n/a
42	chr1:75841810-75841860	NT2-D1	testis:	n/a
43	chr1:75841810-75841860	SKMC	muscle:	n/a
44	chr1:75808730-75808780	NT2-D1	testis:	n/a
45	chr1:75808730-75808780	AG09319	gingival:	n/a
46	chr1:75841810-75841860	NHBE	bronchial:	n/a
47	chr1:75808730-75808780	SK-N-SH	brain:	n/a
48	chr1:75808730-75808780	HCF	heart:	n/a
49	chr1:75808730-75808780	ovcar-3	ovarian:	n/a
50	chr1:75841810-75841860	ProgFib	skin:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:75802617..75804536-chr1:75804779..75807311,2	K562	blood:
2	chr1:75730735..75733136-chr1:75734426..75736968,2	K562	blood:
3	chr1:75934636..75936669-chr1:76193127..76195034,2	K562	blood:
4	chr1:75755636..75758198-chr1:75891029..75893003,2	K562	blood:
5	chr1:75900200..75901997-chr1:75902779..75905400,2	K562	blood:
6	chr1:75731173..75731698-chr1:76097693..76098339,2	MCF-7	breast:
7	chr1:75778138..75780699-chr1:75795597..75797835,2	K562	blood:
8	chr1:75819174..75821466-chr1:76259462..76262137,2	K562	blood:
9	chr1:75770101..75774631-chr1:75777492..75782800,4	K562	blood:
10	chr1:75767207..75769127-chr1:76188046..76189945,2	K562	blood:
11	chr1:75900200..75901997-chr1:75902779..75905400,2	K562	blood:
12	chr1:75887927..75890320-chr1:76006872..76008474,2	K562	blood:
13	chr1:75802617..75804536-chr1:75804779..75807311,2	K562	blood:
14	chr1:75804511..75807217-chr1:75808092..75810770,2	K562	blood:
15	chr1:75756515..75758289-chr1:75759865..75761416,2	K562	blood:
16	chr1:75820905..75823291-chr1:75839784..75841753,2	K562	blood:
17	chr1:75837137..75838827-chr1:75839642..75842194,2	K562	blood:
18	chr1:75730735..75733136-chr1:75734426..75736968,2	K562	blood:
19	chr1:75804511..75807217-chr1:75808092..75810770,2	K562	blood:
20	chr1:75913816..75916653-chr1:75939102..75941877,2	K562	blood:
21	chr1:75756515..75758289-chr1:75759865..75761416,2	K562	blood:
22	chr1:75821210..75823123-chr1:75827154..75829590,2	K562	blood:
23	chr1:75826578..75828663-chr1:75838109..75841105,2	K562	blood:
24	chr1:75837137..75838827-chr1:75839642..75842194,2	K562	blood:
25	chr1:75763247..75766702-chr1:75766779..75769918,3	K562	blood:
26	chr1:75891109..75893224-chr1:75895792..75897457,2	K562	blood:
27	chr1:75755636..75758198-chr1:75891029..75893003,2	K562	blood:
28	chr1:75826578..75828663-chr1:75838109..75841105,2	K562	blood:
29	chr1:75784252..75785931-chr1:75795066..75796962,2	K562	blood:
30	chr1:75891109..75893224-chr1:75895792..75897457,2	K562	blood:
31	chr1:75731104..75731714-chr1:76048302..76048818,2	K562	blood:
32	chr1:75933652..75935311-chr1:76250222..76252176,2	K562	blood:
33	chr1:75778138..75780699-chr1:75795597..75797835,2	K562	blood:
34	chr1:75832449..75834069-chr1:76250552..76252423,2	K562	blood:
35	chr1:75784252..75785931-chr1:75795066..75796962,2	K562	blood:
36	chr1:75830302..75833170-chr1:75834752..75836342,2	K562	blood:
37	chr1:75820905..75823291-chr1:75839784..75841753,2	K562	blood:
38	chr1:75866285..75866785-chr7:55322686..55323666,2	K562	blood:
39	chr1:75821210..75823123-chr1:75827154..75829590,2	K562	blood:
40	chr1:75830302..75833170-chr1:75834752..75836342,2	K562	blood:
41	chr1:75763247..75766702-chr1:75766779..75769918,3	K562	blood:
42	chr1:75770101..75774631-chr1:75777492..75782800,4	K562	blood:

No data

Variant related genes	Relation type
SLC44A5	TF binding region
SLC44A5	CpG island
ENSG00000178193	chromatin interactions
ENSG00000137955	chromatin interactions

Extended variants
information (count: 4341 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:4341 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561315503	chr1:75716676-75716677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573349047	chr1:75716683-75716684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573247924	chr1:75716767-75716768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376766731	chr1:75716799-75716800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559262718	chr1:75716812-75716813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149023216	chr1:75716846-75716847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551300709	chr1:75716851-75716852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs588098	chr1:75716925-75716926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs147564575	chr1:75716927-75716928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114123196	chr1:75716928-75716929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149200222	chr1:75716937-75716938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376030186	chr1:75716945-75716946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200776383	chr1:75716951-75716952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199510718	chr1:75716963-75716964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75019117	chr1:75716994-75716995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539184246	chr1:75717063-75717064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557593519	chr1:75717069-75717070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576007912	chr1:75717126-75717127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377393225	chr1:75717144-75717145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557804578	chr1:75717174-75717175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143023904	chr1:75717217-75717218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148285407	chr1:75717253-75717254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186617540	chr1:75717276-75717277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540290669	chr1:75717298-75717299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565348143	chr1:75717304-75717305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369470688	chr1:75717313-75717314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117215664	chr1:75717385-75717386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556049367	chr1:75717422-75717423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs679018	chr1:75717432-75717433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs563189048	chr1:75717435-75717436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530705572	chr1:75717478-75717479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191317487	chr1:75717490-75717491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560697288	chr1:75717512-75717513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543410177	chr1:75717527-75717528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1394736	chr1:75717542-75717543	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181207028	chr1:75717585-75717586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114672739	chr1:75717637-75717638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115342989	chr1:75717704-75717705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61796540	chr1:75717731-75717732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557057582	chr1:75717755-75717756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77628600	chr1:75717758-75717759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545563247	chr1:75717907-75717908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1394737	chr1:75717914-75717915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536924209	chr1:75717988-75717989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559436722	chr1:75717999-75718000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142869641	chr1:75718027-75718028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113842177	chr1:75718066-75718067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186133851	chr1:75718090-75718091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374995839	chr1:75718181-75718182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534155705	chr1:75718186-75718187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	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
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75711800-75718800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:75716400-75723800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:75718400-75720400	Enhancers	Primary B cells from peripheral blood	blood
4	chr1:75720400-75726200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr1:75723200-75723400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:75726200-75727800	Enhancers	Primary B cells from peripheral blood	blood
7	chr1:75730600-75732200	Enhancers	HepG2	liver
8	chr1:75731600-75731800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:75731600-75732000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr1:75731800-75732800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:75732800-75737200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:75735800-75736000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:75736400-75738400	Weak transcription	Fetal Brain Female	brain
14	chr1:75737200-75737800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:75737400-75737600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:75737600-75738600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:75737800-75743000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:75738400-75740800	Enhancers	K562	blood
19	chr1:75738600-75739200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:75739200-75741800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:75739800-75742400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:75741000-75741800	Enhancers	NH-A	brain
23	chr1:75741400-75741800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr1:75741800-75742000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:75741800-75742000	Flanking Active TSS	NH-A	brain
26	chr1:75742000-75742400	Active TSS	NH-A	brain
27	chr1:75742000-75742600	Enhancers	NHEK	skin
28	chr1:75742400-75742600	Flanking Active TSS	NH-A	brain
29	chr1:75742400-75742800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:75743000-75743200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:75757800-75758000	Enhancers	Fetal Heart	heart
32	chr1:75758000-75759200	Weak transcription	Fetal Heart	heart
33	chr1:75758200-75758400	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr1:75759000-75760600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:75759200-75760400	Enhancers	Fetal Heart	heart
36	chr1:75759600-75759800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr1:75759600-75760400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:75766400-75767200	Enhancers	HUVEC	blood vessel
39	chr1:75766600-75767200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:75770200-75772000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:75770600-75771000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:75770600-75771600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:75770800-75771400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:75771000-75772800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr1:75771400-75774200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:75772000-75773200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:75772800-75773600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:75772800-75774400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:75773000-75774400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:75773200-75774000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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