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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS040-00017
Organism
Homo sapiens
Tissue/cell
Esophagus
Coordinate
chr1:1160390-1161630
Target genes
Number: 28
Name
Ensembl ID
ISG15
ENSG00000187608
C1orf159
ENSG00000131591
TTLL10
ENSG00000162571
TNFRSF18
ENSG00000186891
TNFRSF4
ENSG00000186827
SDF4
ENSG00000078808
B3GALT6
ENSG00000176022
FAM132A
ENSG00000184163
UBE2J2
ENSG00000160087
RP5
ENSG00000230415
SCNN1D
ENSG00000162572
PUSL1
ENSG00000169972
ACAP3
ENSG00000131584
CPSF3L
ENSG00000127054
GLTPD1
ENSG00000224051
TAS1R3
ENSG00000169962
DVL1
ENSG00000107404
MXRA8
ENSG00000162576
AURKAIP1
ENSG00000175756
CCNL2
ENSG00000221978
RP4
ENSG00000224870
MRPL20
ENSG00000242485
ANKRD65
ENSG00000235098
VWA1
ENSG00000179403
ATAD3B
ENSG00000160072
ATAD3A
ENSG00000197785
SSU72
ENSG00000160075
MIB2
ENSG00000197530
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr1
1160713
1160888
chr1
1161319
1161601
Enhancer Sequence
ACCACAGACT TGGGGGATAG GGACACAGAC TGGGGACACG GGGCCAGCGC AGGCCAGGTC 60
AGGAGGCCAC AGGCCCCAGG ACAGGTCACT CCCGTCCCAG CTTCAGAGCT CGGCTTCACC 120
ATTATGTCTT TGTGGAAGCC ACAGGCTCCT ACCCCTGCTG CAGCCGCCCG TGTCCTGAGC 180
TCACCTGTTG GAAACTTAAC CCCCAGGGCA ACAGCACTGG GAGGCAGGGC TTCCAGAGGT 240
GCGAGGTCTT GAGACCCCGG CTGGTGCGTT TGCCGGAGGC ATCCCCGAGA GTAGGGTGCC 300
CTGGCCCCTT GCCTCTATGC TCCGCTCAGG GGCAGCCGCG GCCACGTTAT GAGGTGGCAA 360
GCAGGCCCTC GTCAGGCAGG TGTGGCCTCT GGGACCTGGG CCAGGCAAGC TTCGAGGGTG 420
CACACACCGC AGGCACGGCT CAGAAGCACT GGGCAGAGAT CCTCATGGAA GAAGGCCAGG 480
CTGCCGCTCA CACGCGCCCC TCCCTCAGCA GCCGCAGCAG CCCAGAGGTG GACGGGCCTG 540
GGAGGCACCC TCAGCTCCAC AGTCCCCAAA ACACACCGGC TGGGGACGGG GCCACCCGGG 600
TGGCCATGTG GCAGGTGGGG CACCTGGTGG GTCTCACGTG GACACGTGCA TCCTCGAATG 660
CTCCGGTCAC GCTCCACACG CGCCACAGAC ACAGGCCACA CGCTCCACAC GCCACAGACA 720
CGGGCCACAC ACTCCACATG CCACAGACAC GGGCCACACA CTCCACACGC TCTACACACT 780
CCACAGACAC AGACACACAC GAGGCAGAGC AAAAAGCAAA AAGGTGGAAA GAAACCACAT 840
GGCGCAGGAT TCCAGTCAAG ATGTCGGCAA GGAGTCACTC ATCCAAACTC AGGTGCCTGA 900
AGACACGGCT GCAGGGCGGT GCACGTACAT GGAGCTGGCA CGCACACACG CAAGTGCACA 960
GGCCGGTACC CACGTGTACA CAGCACACAC ACGTGAACAG GGCTGGCAGA ACACAGATGT 1020
GACTGGGCTG GTGCACACAC GCATGTTATC AAGTTCTGGC TCCTGAGAGA ACAAGGGCAA 1080
GACGCCCAGT GCCCAGACCC TGGCTTCCAG CTCCAGCCAC GGGAGACAGG GCTTCCTGGA 1140
AAGGCGGCAG CTATTGCACT GGGGCAGGTG GCACGGAGGC GAGCCCAGAG CATCTCACCG 1200
TGCCAGGAAG CGGGAAGGAA AGCCTGGAGC ATCTCGTGGT 1240