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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS133-21448
Organism
Homo sapiens
Tissue/cell
melanoma
Coordinate
chr22:38523000-38524270
Target genes
Number: 40
Name
Ensembl ID
RP1
ENSG00000235237
Z82188.1
ENSG00000255594
RAC2
ENSG00000128340
CARD10
ENSG00000100065
CDC42EP1
ENSG00000128283
GGA1
ENSG00000100083
SH3BP1
ENSG00000100092
Z83844.1
ENSG00000233360
PDXP
ENSG00000241360
LGALS1
ENSG00000100097
NOL12
ENSG00000256872
TRIOBP
ENSG00000100106
H1F0
ENSG00000189060
GCAT
ENSG00000100116
ANKRD54
ENSG00000100124
EIF3L
ENSG00000100129
MICALL1
ENSG00000100139
POLR2F
ENSG00000100142
C22orf23
ENSG00000128346
SOX10
ENSG00000100146
RP5
ENSG00000222044
PICK1
ENSG00000100151
SLC16A8
ENSG00000100156
BAIAP2L2
ENSG00000128298
PLA2G6
ENSG00000184381
MAFF
ENSG00000185022
AL021977.1
ENSG00000256873
TMEM184B
ENSG00000198792
CSNK1E
ENSG00000213923
RP3
ENSG00000244627
KDELR3
ENSG00000100196
DDX17
ENSG00000100201
DMC1
ENSG00000100206
CBY1
ENSG00000100211
TOMM22
ENSG00000100216
JOSD1
ENSG00000100221
GTPBP1
ENSG00000100226
PRDX3P1
ENSG00000229598
AL021707.1
ENSG00000203583
DNAL4
ENSG00000100246
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr22
38524042
38524152
chr22
38523184
38523224
Enhancer Sequence
TGGCCTCCGG GATCAGGCCC ACCATCCACT CTGTCCATGT CTTCCTTTGT GTCCAAGGCC 60
TGCCTGACGT CCACCCAACT GACTAGCTGC CCCTCCTGAC AAGCAGCCCA GTCCCCAGGT 120
GCCTGGTGCA GCAGCCCGCG TGACCCCAAC TCTGACAGCC CCCCACCACT GTGCAGAGTC 180
TAGAAGCAGC AAAGCAGAAC CGAGGGCTGC GAAGCGGTGT CTCCCCCTCC CCAGGGCACA 240
CGGCTCCACA GTGAACAAGG GAAGCAGAAG AGTGGCTGAG AGAGGCCGGG GACAGGGTGC 300
AGGGGAGGGG GCGTGTGGTG TGTGCGCAGC TAAGAAGGAC GGATTAGGGA GTGAGAGCTA 360
GAGCTAATGC CGCATGGCTA GGCTCGGTGG CCTCTCCAGG CCCAGGGCGT TACCCATCTG 420
ACGCCGCACC CCAGGCCCAC CATCCGGCCT GGCTTGGGTG ACTGCCTGCA AAATTGAGAG 480
ATAAAGATGG GAGGTGGAGG GGGAGTTCCT GGGAGGGGAG AGAGAGGTGG AGCCAGGACT 540
AGAAGCCACA GTCACGGTGC CTCTCCAGAG TTCCAGGCTT GGTCGGGCTA CCCTGGCTGA 600
AGGTGCTGCC GCCTCCACAG TGAAGTCTGG CTCACCAAGG ACTGGCTCCT GGCTGCCCTC 660
TGTTCAGGGG ACCCCGCTCC CAAACAATGG AGGTCCCTGA GTGGGCCAGC CCACAGAAAG 720
TCCAGAGAAG GGTCCTGTCT AGTCTGGGGA TGTCTCCCTG GGCACCAAGG AATGCACCGG 780
GGCAGATGCT GGCTGCCTGG CCACATTCAA CGTCTGAAAG TCACCACGGG GCCAGGAAGG 840
GGGCACACAG GTCTCAGGCC CAACCGAGAT TCAAACAGTG TGATAGAGGT GAAGCCAGAG 900
GGACAGGTGA AGCCAGAGGG CCCGGGCCCC CAGTCCCCCG ACAGCACTCC TCACTGCCCA 960
CCCTGAACGC CCTGGGGACA GGAGGGCAGT AACAGCAGCC ACCTCATGGG TGCCACTGGA 1020
AATGCCCAGG CCTGAGACTG TGTGCAGGAC ACATCCTCTC AGGGGCAACG GAGCATGGGA 1080
CATCAGCCAG GGACACCCTA GGCCTCTGGG ATCTGTGGGT TGCTGGCTGC CTAGAGGCTG 1140
ACAACTCCGG CCCCATCCTC CCCGGCTTCC TTTAGTGACT TCCGTCCTAG GGATCCTGTT 1200
GCTTTGGTGG GGCCTGCTGT GATCCAGGGG CCTGGGAACC AGCTGGAGAA GAGGGAGTCG 1260
GGAGGCGAGG 1270