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

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EnhancerAtlas ID
HS050-27581 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr17:7195370-7196790 
Target genes
Number: 57             
NameEnsembl ID
RPL7AP64ENSG00000213876
ASGR1ENSG00000141505
ACADVLENSG00000072778
DLG4ENSG00000132535
MIR324ENSG00000199053
DVL2ENSG00000004975
PHF23ENSG00000040633
GABARAPENSG00000170296
CTDENSG00000262526
C17orf81ENSG00000170291
CTDNEP1ENSG00000175826
RP1ENSG00000262302
CLDN7ENSG00000181885
YENSG00000202251
SLC2A4ENSG00000181856
YBX2ENSG00000006047
EIF5AENSG00000132507
GPS2ENSG00000132522
RP11ENSG00000261915
NEURL4ENSG00000215041
AC026954.6ENSG00000224647
ACAP1ENSG00000072818
KCTD11ENSG00000213859
TMEM95ENSG00000182896
TNK1ENSG00000174292
C17orf61ENSG00000262481
PLSCR3ENSG00000187838
NLGN2ENSG00000169992
SPEM1ENSG00000181323
C17orf74ENSG00000184560
TMEM102ENSG00000181284
FGF11ENSG00000161958
CHRNB1ENSG00000170175
ZBTB4ENSG00000174282
POLR2AENSG00000181222
TNFSF12ENSG00000239697
TNFSF13ENSG00000161955
SENP3ENSG00000161956
EIF4A1ENSG00000161960
SNORA48ENSG00000209582
SNORD10ENSG00000238917
SNORA67ENSG00000207152
CD68ENSG00000129226
MPDU1ENSG00000129255
AC113189.5ENSG00000233223
SOX15ENSG00000129194
snoU13ENSG00000251860
FXR2ENSG00000129245
SAT2ENSG00000141504
ATP1B2ENSG00000129244
WRAP53ENSG00000141499
TP53ENSG00000141510
EFNB3ENSG00000108947
RPL29P2ENSG00000240480
CHD3ENSG00000170004
LSMD1ENSG00000183011
TRAPPC1ENSG00000170043
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr17:7196013-7196034GGGGGAGGGGAGAAAGGAAAA+7.1
Enhancer Sequence
TGTCATTCCT GCAGAACAGG ATGGGTCGTT AAGGAAGGGA CTTCAACAAA GCCCTCAGCT 60
CCTCACTGAG GTCCCCCTAG ATGCCCAGTC TAAGCTCAGT GGGCCCATCC TCTCCAGCAT 120
TCCAGTTAGG GGTGGACATG GCCTGGGGAA TGGGAGGGAG AGCCAGCAGG GCCCCCAGAA 180
GCTGGTGTAA AGAGAGATAC ACCTAAAACC TCAGTGCCAA ACCTGGACTT CACAAGGAAA 240
GGGCAGGCTG GGGAGGCAAA GGCACCTTGA GGAACCTCAG ACAGCTCTGC CCCTGCCGGG 300
ACTCCACCTT CCACCCCAGG CTAGCCTTAC AACCTGCCAG CGCTGGGTGC AACTGTCCCT 360
GGCCAACACC CCCTCCCCCA ACCCCCATCA GGGTTGGAAA ATTCCAGTCT TCTTCCTTCT 420
ATAGTCAAGG AGGCAGAAAG TGCAGATGGG GCCAGAGGGG CAGAACAAGT TTGAGAAGGG 480
AACAATGTGT CAGGAACTTG CTCTAAACAG CTGCCAAACT TTATTCTCAT CCTCAGCCTG 540
GAGGTGAATC CCAGAGTCAG GACCACTCTC AACACGCGTG GGACCAAGGG TGAGAGAGAA 600
GAAAACATTC ACCCATTCTC TATCATAAGA ACCCCAGTGG GTGGGGGGAG GGGAGAAAGG 660
AAAAGTTTTC CTGGAGGCAC TCTGCCCCCG ACCCAGTCTG CCATTTCCAG AATTAGACAG 720
GGACCCTTCC CCAGAACAAA CGTTTTAGCT TTAAAGCACT TGGATCTGCA CAAAGGTCAG 780
CCTGCTAAGA GGGAACTAGG GCCTCCCAGG AGAGCCAGGC CGGGCAGGAT GCCTGGGCTG 840
GGGAAGGGCC CACTGGGGGA GACCTGGCTC TGCTCAGAAT CCACTGCCAC AGCCTCTCCC 900
GGTGCTGAGG GGTGGGGCTG CCTACTGAAG GAAAGCAGCA GCCTCTGGCT CCTTCCTCCT 960
GACCCCCACT GTCAGCCTCA GTCCCAACAG GTGGAGGGCT CGAATGAGCC ACAGCTCTTT 1020
AAGGGAGTTG AGTTGTGAGT GCTGCCATAA CAGGAAATCA GTTGAGGATT CCAGCCGGGG 1080
GCCCTGAGGC ACAGAGAACC CTATAATACA TTCTGCCCCA AAGGCATGTC AGAGTAAAAG 1140
TAATGAAGCA ATTCCAGAAG GTGAGATGAG AAGCTGGCAG GGTCAGAGCC AGGTTTGCCA 1200
AGTTCCTGAA TCATTAATCC TCCGCTACCC TTGAAGATGC GGAGGAGGCT TCCTCTTGTC 1260
ACGAAGCACA CATTTGTGCT GCGGTTAAAG GCTTTCAACC AGCATCAGCT GGACATTGCA 1320
ACCATGTGCC TCCGCAGGGG TCGATGAGGT TGGGCGGGTG TCCAGTCCCA CAGGCCAGCT 1380
GGGAAGACAC CCATTCCACC CCCGCCCTGG GTTCCTTGGA 1420