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

TagContent
EnhancerAtlas ID
HS060-14078 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr17:7455620-7456610 
Target genes
Number: 39             
NameEnsembl ID
TXNDC17ENSG00000129235
RP11ENSG00000262089
RNASEKENSG00000219200
ACADVLENSG00000072778
DLG4ENSG00000132535
C17orf81ENSG00000170291
CTDNEP1ENSG00000175826
EIF5AENSG00000132507
GPS2ENSG00000132522
NEURL4ENSG00000215041
ACAP1ENSG00000072818
TNK1ENSG00000174292
C17orf61ENSG00000262481
PLSCR3ENSG00000187838
TMEM102ENSG00000181284
FGF11ENSG00000161958
SLC35G6ENSG00000259224
ZBTB4ENSG00000174282
POLR2AENSG00000181222
TNFSF12ENSG00000239697
TNFSF13ENSG00000161955
SENP3ENSG00000161956
EIF4A1ENSG00000161960
SNORA48ENSG00000209582
SNORD10ENSG00000238917
SNORA67ENSG00000207152
CD68ENSG00000129226
MPDU1ENSG00000129255
AC113189.5ENSG00000233223
SOX15ENSG00000129194
SHBGENSG00000129214
FXR2ENSG00000129245
SAT2ENSG00000141504
ATP1B2ENSG00000129244
WRAP53ENSG00000141499
TP53ENSG00000141510
VAMP2ENSG00000220205
SNORD118ENSG00000200463
AURKBENSG00000178999
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1774560677456382
chr1774559487456460
Enhancer Sequence
AGGAGTCATG GCCATATGGA TGGCTTTTTT TTTTTTTTTT TTGAGACAGA GTCTCGCTCT 60
GTCACCCAGG CTGGAGTGCA GTGGTTCGAT CTTGGCTCAC TGCAACATCT GCCTCCTGGG 120
TCCAAGCGAT TCTCCTGTCT CAGCCTCCCA AGTAGCTGAG ATTATAGGCG GGTGCCACCA 180
CACCCAGCTC ATTTTTGTAT TTTTTAGTAG AGACAGGGTT TCACCGTGTT GGCCAGGCTG 240
GTCTTGAACT CCTGATCTCA GGTGATCCGC CAGCCTCAGC CTCCCAAAGT GCTGGGATTA 300
CAGGTGTGAG CCCTTGTGCC CGGCCTATCG ATGGCATTTA AAGCCACAGG ATTGGGTGAG 360
ACGCCAGGAG AAAGAAGGGC CCCACGAATG AAGCCCTGAG ACTCTTGGGC ATCTTGAAGT 420
GGAGCTGAGG GGAAAACCAG CAGAGACTGA AAAGAAGCTG GAGAGAGAGG AAGAAACCCA 480
GGGAGGGTGG CATCCTGGAT TCGGAGAAAC CACTGTTTCA AGGAGGATGT GGCTGTCTGT 540
GTTGAATGCA GCTGAGAGAT CACATGAAAT GAGAACAGAG AAATGATGGC TGGGTTTGGT 600
AACGTGAAAG TCCTGCTGAC CTTAAAGAGG GTGGTTTCAG TGGCATAGTT AGAACAGGAA 660
GGCAGTGTGC ATTGGGTTGA GAAGAAAATG AGAAATAAGG AACTGGAGGC AGGGACAACC 720
TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTG TGACAGAGTT TCACTCTTGT 780
CACCCAGGCT GGATCCAGTG CAATGGCACG ATCTCGGCTG ACCGTAACCT CCACCTCCCG 840
GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC CCAGTAGCTG AGATTACAGG CATGCGCCAC 900
CACGCCTGGC TAATTTTGTA TTTTTAGTAG AGACAGGGTT TCTCCATGTT GGTCAGGCTG 960
GTCTCAAACT CCCGACCTCA GGTGTTCCAC 990