EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

EnhancerAtlas 2.0

Tag

Content

EnhancerAtlas ID

HS088-03544

Organism

Homo sapiens

Tissue/cell

HeLa-S3

Coordinate

chr1:150480760-150482000

Target genes

Number: 21
Name	Ensembl ID

ANP32E	ENSG00000143401
U2	ENSG00000222222
TARS2	ENSG00000143374
ECM1	ENSG00000143369
LINC00568	ENSG00000228126
ADAMTSL4	ENSG00000143382
AL356356.1	ENSG00000225996
C1orf138	ENSG00000203804
MCL1	ENSG00000143384
SNORA40	ENSG00000253047
ENSA	ENSG00000143420
GOLPH3L	ENSG00000143457
HORMAD1	ENSG00000143452
CTSS	ENSG00000163131
CTSK	ENSG00000143387
ARNT	ENSG00000143437
RP11	ENSG00000224800
SETDB1	ENSG00000143379
CERS2	ENSG00000143418
CDC42SE1	ENSG00000197622
SCNM1	ENSG00000163156

TF binding sites/motifs

Number: 1

JASPAR ID

Coordinate

Motif Sequence

Strand

-Log10(p-value)

Crx

MA0467.1

chr1:150481850-150481861

GAGAGGATTAG

6.02

HEDD

Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome	Start	End

chr1	150481400	150482000
chr1	150481671	150481757

Enhancer Sequence

TTGGGGGATC AGCACTTAGG AGGGGGTCTG GGCTTGCATG GCAGGGGTCT GGGTCCAGGC 60
ATCCCAGACG GCTCATCACT AGCAGAGTGA TTCTCCGTTT GGCTTTCCTT TTCTGAGCAG 120
GCCCAAAGTG GGCCTAGGCC AGTGGAGCCT TTAACCAAGG AGGCAGAGAG CAGGGGCACA 180
GAAGGAGAGG GGTTCCTAGA AACTGCTGCC AAGAAACACA GAATCCCAGT CAAATAGACA 240
ACTGAGTGGG GGGTGGGTTC ACAGAGTGAG GGTCTCCTGC TGATGAGGAT GTAGGGAGGT 300
GGCTGGTGGG AGAGGCAAGG GAGGGAAAAG GGGCCCCCAG GCTGCTCAAA ACCGGATTGC 360
TGGCCCAGCA AGCCTCGACT GACTCCCTGT CTGATTAGAG GAGTTGAGGG GTGTCCATCC 420
ACAGACCCAC CCTCCATCCA GCACAAACAC ATTCTTTATC TGCTTTGATG CCTGAACAAA 480
ACAGGAACCC CTCAATGCTA TGGGTGGAAA CTAAGAAAAA AAGGAAAAGA AAAGGAAAAA 540
AACCACCCAG GGCACTCCTG CAGGAAGCTG CTGAGGATGT CAGCAAATCT GTCCACTTCT 600
CTGTGAAGCC CCATGCCATC ATTCTTCCCA GCTCCTGGTC TTTTGTGTCT GCAGATCACC 660
TACAAGTGAC CCTTCCCTGT GCCTGTCCCA GTCCCCCAGG CCCTAAATTG AGACCTAAAC 720
TAAGGCGGAG CTGAGACTGG CTGAAGGGGA AGCACTCAAC CTTCAGGAAG CCTCCTTAAC 780
CAAAGGCCTA AAGATGTTTC AAGGGCCTGG AGTAGGAGGG TGGGTGGAGG AGGTGGATTG 840
GGTAGGCTCC AACCAGCTCA AGGTCCAGAC TTTTTCCTCT GAAAGCTAGA GACGCATCCC 900
AGCAGAGACT GGGGAGGACA ACCCACAGCC CTGAGGGAAA GACTGGCAGA GGAAATGAGG 960
GCCTCCCTCC CCAATCCCGT ATGCCATACT CCCTTTAGGC CCAACCTCTG AGCCAGTAGA 1020
GGTGGAGCTA TCAGACCGCC ACAGGCTTTC TCAGAACCCA GCTGGTCATG TCTAGGTGTG 1080
TTGGGGCTGG GAGAGGATTA GGGGACACGG GGCAGGTGAA TACAGAGGGG CATCTCGTGT 1140
CTTGCTTGTC TGTCCTACAC TCTTGATCTC CACAGCCTCC CCATCCCTTG CTGAAGTCCA 1200
GGGAAGGCCC TCCCAGTGGC CCCTGACTTG CCCTTCTTCC 1240