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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS105-85666
Organism
Homo sapiens
Tissue/cell
IMR90
Coordinate
chrX:153733520-153734480
Target genes
Number: 34
Name
Ensembl ID
HCFC1
ENSG00000172534
MECP2
ENSG00000169057
XX
ENSG00000231830
FLNA
ENSG00000196924
EMD
ENSG00000102119
RPL10
ENSG00000147403
SNORA70
ENSG00000207165
TAZ
ENSG00000102125
DNASE1L1
ENSG00000013563
BX936347.1
ENSG00000197180
ATP6AP1
ENSG00000071553
GDI1
ENSG00000203879
FAM50A
ENSG00000071859
PLXNA3
ENSG00000130827
LAGE3
ENSG00000196976
UBL4A
ENSG00000102178
SLC10A3
ENSG00000126903
FAM3A
ENSG00000071889
WI2
ENSG00000261773
IKBKG
ENSG00000073009
G6PD
ENSG00000160211
ATF4P2
ENSG00000231342
CTAG1A
ENSG00000183678
CTAG1B
ENSG00000184033
ATF4P1
ENSG00000213338
CTAG2
ENSG00000126890
AF277315.13
ENSG00000226141
DKC1
ENSG00000130826
SNORA36A
ENSG00000206948
SNORA56
ENSG00000206693
HMGN1P26
ENSG00000229237
MPP1
ENSG00000130830
F8A1
ENSG00000197932
FUNDC2
ENSG00000165775
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chrX
153734147
153734434
chrX
153733846
153733919
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH0XI154505
chrX
153733788
153735035
Enhancer Sequence
GTCCAAACCC ACTGAACGTC CAACAGCAAA CTGAAGCCTC ATGTGAGCAC CGATACTGGT 60
TCATTGACAG CAACAGATGG GAAGCTGGGG GCTGGCAGGG GGCACACAGG AACTCTGACC 120
TTTTCACTCA GTTTTGCTGT GAACCTAAAA TGGCTCTAAG AAGGAAAGTT TACAAAAACA 180
AAAAAGGAAT GGAATACACG TAGAAAGTTC CTGGTGCAGA GGCAGGACTG GCATCACCAT 240
CGTTTCCTCC CTGGTGAGCC GCTCCTCCAG GGCACCCCTG TGCCTCCAAC CCCACATGTG 300
CCTGCTCCAG AAGCACTTTT GTCTTCTGAG GCTCTGTCTG CGCTCTGTAC TCTTCCTGGG 360
ATTGGCTCCT AAGTCCATCG CCCCTAACGT CGCCCCATGA AGGACACCAC AGTGCCTCCC 420
ATCTAGGAAC TGCCTTCTCT CCTTTCGCTG AACTCAGACT GCTTCTGGGC CTCTGGAGTT 480
GATATTCCAG CAAAATTGCT TCTAATTTGC TGGCTCTCGC TTAGCAAAGG GAGGTATTAA 540
CCGTAACCTG GGAGAGACGC AAAAAGCCCA AGTGACTCGA CCCCTCACAA CCCTGACTTC 600
AAAGGCAGCC GAAGTCTGTG GGCGACATGT GCTCCTGGAT GATGATGGGG TGTGGTGGGG 660
GCCTGGGCTG GTGTTAATCC CAATCCCTGT CCCTGTCCGT ACAGGCCTGC ACTGGGTCAG 720
AGGGAGTTGT TGAGTCAGCT TCCTGCAGCC CGAGTGTGCA ATCTTCTCTG CCAGACGAAA 780
AGAGTCCCAC TGCTCTGTTG ACTGCTTGAG TCACATCTCA GTCGCAGCGG GGCCTGTTGG 840
TGGCAGGAGC CCTGGAGACA AAAGGCTGTC TGCTCGGGCT GTGGGAGCAG GTTGGTTAAG 900
ACTCTGGAAT CTGTCCTCCC GCACCCCAGA GGACACCGCC ACCTCTGACT CCGCACTGAC 960