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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS197-13928
Organism
Homo sapiens
Tissue/cell
ZR75-30
Coordinate
chr22:38204170-38204830
Target genes
Number: 32
Name
Ensembl ID
RP1
ENSG00000243902
ELFN2
ENSG00000166897
MFNG
ENSG00000100060
CARD10
ENSG00000100065
CDC42EP1
ENSG00000128283
GGA1
ENSG00000100083
SH3BP1
ENSG00000100092
Z83844.1
ENSG00000233360
PDXP
ENSG00000241360
Z83844.2
ENSG00000241333
LGALS1
ENSG00000100097
NOL12
ENSG00000256872
TRIOBP
ENSG00000100106
H1F0
ENSG00000189060
GCAT
ENSG00000100116
GALR3
ENSG00000128310
MIR658
ENSG00000207945
ANKRD54
ENSG00000100124
EIF3L
ENSG00000100129
MICALL1
ENSG00000100139
POLR2F
ENSG00000100142
C22orf23
ENSG00000128346
SOX10
ENSG00000100146
PICK1
ENSG00000100151
RP5
ENSG00000233739
SLC16A8
ENSG00000100156
BAIAP2L2
ENSG00000128298
PLA2G6
ENSG00000184381
MAFF
ENSG00000185022
AL021977.1
ENSG00000256873
TMEM184B
ENSG00000198792
CSNK1E
ENSG00000213923
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr22
38204433
38204600
Enhancer Sequence
GTAACGCTCC GTTCCGGGAG TCGTTCCAAG ACCTTTCCCG AGCTTGCGCT GGAATGGAGG 60
TCCTGGAGGT GGGGGTGGGC GGCTCCTACA CTCTTAGCTA CTGTTCCCCT TCGCATCTCT 120
CAGGGCGACT TTATGGCTTC CTAATATTGA CTCTTGCCTG GTTAAACCCT TTTGACGGAG 180
GGAGGCGATT TGCCCAGCAA GAAAACCCGC ATTTCTTGAG CGGCTCCTTT GTGAAGGTCT 240
CTACCAATTG TTGCTGCACG TGAACTCCTG CTAACTTCTA GACGCAGGAA TGACTAATTC 300
CACTTTACAA ACGAAGAGGC TGAAATCCAC AGATGTGAAA TGGCTTGCCC AAAAGCCCCC 360
AGCTAGCTGC AGGCAGCGCT GGAATATTGG AGCTGGAACA TTGCCTGACT GGCCAGAGAG 420
GACAGCTTGC TGGGTAAACT CATAGCAAGC AAGGGGTCCC AGGGCTGCCA CAGAAATCAC 480
ATGATGAGTT GGCCCTGCCA GGTCTCCCTC ATTTCTTTCT TTCCTTTTTT TTTTCTGAGA 540
TGGAGTCTCG TCTTGCTCTG TCGCCCAGGC TGGAGTGCAG TGGCGAGATC TCGGTTCACT 600
GCAACCTCTG CCTCCCGGGT TCAAGCGATT TTCATGCCTC AGCCTCCCAA GTAGCTGGGA 660