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

TagContent
EnhancerAtlas ID
HS088-03795 
Organism
Homo sapiens 
Tissue/cell
HeLa-S3 
Coordinate
chr1:155202330-155204230 
Target genes
Number: 40             
NameEnsembl ID
ADARENSG00000160710
KCNN3ENSG00000143603
PMVKENSG00000163344
PBXIP1ENSG00000163346
PYGO2ENSG00000163348
SHC1ENSG00000160691
CKS1BENSG00000173207
FLAD1ENSG00000160688
LENEPENSG00000163352
ZBTB7BENSG00000160685
DCST2ENSG00000163354
DCST1ENSG00000163357
RP11ENSG00000232093
ADAM15ENSG00000143537
EFNA4ENSG00000243364
EFNA3ENSG00000143590
EFNA1ENSG00000169242
SLC50A1ENSG00000169241
DPM3ENSG00000179085
HMGN2P18ENSG00000223452
TRIM46ENSG00000163462
KRTCAP2ENSG00000163463
MUC1ENSG00000185499
MTX1ENSG00000173171
THBS3ENSG00000169231
GBAP1ENSG00000160766
MTX1P1ENSG00000236675
AL713999.1ENSG00000216109
GBAENSG00000177628
FAM189BENSG00000160767
SCAMP3ENSG00000116521
HCN3ENSG00000143630
CLK2ENSG00000176444
PKLRENSG00000143627
FDPSENSG00000160752
RUSC1ENSG00000160753
ASH1LENSG00000227773
snoU13ENSG00000238805
DAP3ENSG00000132676
YY1AP1ENSG00000163374
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EHFMA0598.2chr1:155202842-155202854GACCCGGAAGTG+6.07
ELF1MA0473.2chr1:155202842-155202854GACCCGGAAGTG+6.44
ELF3MA0640.1chr1:155202842-155202855GACCCGGAAGTGG+6.12
ELF4MA0641.1chr1:155202842-155202854GACCCGGAAGTG+6.52
ELF5MA0136.2chr1:155202843-155202854ACCCGGAAGTG+6.32
ZBTB7AMA0750.2chr1:155202843-155202856ACCCGGAAGTGGT+6.21
ZNF263MA0528.1chr1:155204094-155204115TGAGGAGGATGAAGAGGAATG+6.19
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_27291chr1:155200942-155205410Esophagus
SE_68020chr1:155161591-155248159TC32
SE_68021chr1:155161591-155248159TC32
SE_68022chr1:155161591-155248159TC32
SE_68023chr1:155161591-155248159TC32
SE_68024chr1:155161591-155248159TC32
SE_68025chr1:155161591-155248159TC32
SE_68026chr1:155161591-155248159TC32
SE_68027chr1:155161591-155248159TC32
SE_68028chr1:155161591-155248159TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1155202484155202779
Number: 1             
IDChromosomeStartEnd
GH01I155231chr1155201192155202850
Enhancer Sequence
GACGGCCAGC GGGCTCCAAG GCCCAGGCTT TTTGCCAACA GCAACAGGCT ACTGGCTGGG 60
CCCAGGCAAG GGGGCCTTGG CAGGAAAAGT TCCTTGCTGT ACCTCCACTG CACTCAGAGG 120
CCAGTGAGGG GGGTACCAGA CAGGACTCCT TCCTCCCTGG TGAAGTGCCC TTGCAGCTCC 180
CCAGCGTCCA CGCCATGGAT ATTTCCTCCA CAGAAGTACA ATGCTGATTA TGATCTGTCA 240
GCTCAGCAAG GGGCAGACAC CCTGGCCTTC ATGTCTCTCC TGGAGGAGAA GTTGATCCCG 300
GTGCTGGTGA GTGTGCCCAG ACCTCCCAGC ATCCATGGCC AGCCGGGGAG GGGACGGGAA 360
CACACAGACC CACACAGAGA CTCAGGAGAG CATGGAGGTC AGAAGCCCAC CTTGAATCAG 420
ACAGGTGCAC TGGCTCAGAC CTGCCTGTTT CTTCCTGCCC ACCCAATCCA GGTACATACT 480
TTTTGGATAG ACACCAAGAA CTACGTAGAA GTGACCCGGA AGTGGTATGC AGAGGCTATG 540
CCCTTTCCCC TCAACTTCTT CCTGCCTGGC CGCATGCAGC GGCAGTACAT GGAACGGCTA 600
CAGCTGCTGA CTGGGGAGCA CAGGCCTGAG GACGAGGAAG AGCTGGAGAA GGAGGTAGCT 660
CTGAGACCGG GGGCTATTGT ATGAGATGAG CCCCAAGGAT GCTGGCCAGG AATGGGAGTG 720
CTTAGGTGCG GAGGTGGCAC TGTTCCCGCA GCTGCAAGCC TACCTGTGTC GCCCCTACAG 780
CTGTACCGAG AGGCTCGGGA GTGTCTGACC CTGCTCTCTC AGCGCCTGGG CTCTCAAAAG 840
TTCTTCTTTG GAGATGCGTG AGTCTGACTC CAAGAGGGTA ATGGGTGGCT TGGAAGAAGA 900
TACAGGTTCA GATGGAGCAG CTGGAGCTGG GGCTGGGGCT GGGGCTGGCT CAGGCTCTGG 960
ATAGGAGGTC CCTGAGACAG ATACTGGCCC TGGTGACAGT GGGGCTGTGC GTGGGGCCAG 1020
AGCCTTCTCA GAGGTACAAA AGGGTAGGGT GGGAGGGCAG CCAGGCACAG GAAGGGCCTG 1080
AAGAGCTGTG GGGCACTGAG TGTGCCCTTT ATGCAGCCCT GGGATAGAGC CCTATTCAGG 1140
GCCAGGCTGG CGCCACCTGG GGATCTCTCC CCATACCAGG TCTAGAACTG TGTGTCCTGT 1200
CCTTCCCTGG TGGCCGCCTG CTGCCCAGAG CCCACCTCCC AAGGCTGACT CTTCCTCCAG 1260
CTCCATCTTT ACCCCTTCTA CCCCAGTGGT TCTCCTCCAT CCCACCCTTC TCTCTCTGCT 1320
CCAGCCCTGC CTCCTTGGAC GCCTTCGTCT TCAGCTACTT GGCCCTGCTG CTGCAGGCAA 1380
AGCTGCCCAG TGGGAAGCTG CAGGTCCACC TGCGTGGGCT GCACAACCTC TGTGCCTATT 1440
GTACCCACAT TCTCAGTCTC TACTTCCCCT GGGATGGAGG TAAGGGGCAG ATGGGAGGGG 1500
CAGCCCTGGG GAGAGTGGGC AGGGATCCAA GAACTAGTTC TCCTAACACA CCTTCCTTCC 1560
TTGACCCTCA GCTGAGGTAC CACCGCAACG CCAGACACCA GCAGGCCCAG AGACTGAGGA 1620
GGAGCCATAC CGGCGCCGGA ACCAGATCCT ATCTGTGCTG GCAGGACTGG CAGCCATGGT 1680
GGGCTACGCC TTGCTCAGCG GCATTGTCTC CATCCAGCGG GCAACGCCTG CTCGGGCCCC 1740
AGGCACCCGG ACCCTGGGCA TGGCTGAGGA GGATGAAGAG GAATGATTTG TCCTCACGCT 1800
CCCAAGACTG GTTTTTCTAC TCTCATGCAT TCCAGAGGCC CCCGTGCCTC CTCGTTGTTG 1860
GTACAGCCGG ACACGGGGTG CTGCCACCCA GAATAAAGCC 1900