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

TagContent
EnhancerAtlas ID
HS076-23674 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr17:7315520-7317660 
Target genes
Number: 72             
NameEnsembl ID
TXNDC17ENSG00000129235
RP11ENSG00000263316
ALOX12ENSG00000108839
RNASEKENSG00000219200
C17orf49ENSG00000161939
MIR497HGENSG00000215067
BCL6BENSG00000161940
SLC16A13ENSG00000174327
SLC16A11ENSG00000174326
CLEC10AENSG00000132514
ASGR2ENSG00000161944
RPL7AP64ENSG00000213876
ASGR1ENSG00000141505
ACADVLENSG00000072778
DLG4ENSG00000132535
MIR324ENSG00000199053
DVL2ENSG00000004975
PHF23ENSG00000040633
GABARAPENSG00000170296
CTDENSG00000262526
C17orf81ENSG00000170291
CTDNEP1ENSG00000175826
RP1ENSG00000262302
CLDN7ENSG00000181885
SLC2A4ENSG00000181856
YBX2ENSG00000006047
EIF5AENSG00000132507
GPS2ENSG00000132522
NEURL4ENSG00000215041
AC026954.6ENSG00000224647
ACAP1ENSG00000072818
KCTD11ENSG00000213859
TMEM95ENSG00000182896
TNK1ENSG00000174292
C17orf61ENSG00000262481
PLSCR3ENSG00000187838
NLGN2ENSG00000169992
SPEM1ENSG00000181323
C17orf74ENSG00000184560
TMEM102ENSG00000181284
FGF11ENSG00000161958
CHRNB1ENSG00000170175
SLC35G6ENSG00000259224
ZBTB4ENSG00000174282
POLR2AENSG00000181222
TNFSF12ENSG00000239697
TNFSF13ENSG00000161955
SENP3ENSG00000161956
EIF4A1ENSG00000161960
SNORA48ENSG00000209582
SNORD10ENSG00000238917
SNORA67ENSG00000207152
CD68ENSG00000129226
MPDU1ENSG00000129255
AC113189.5ENSG00000233223
SOX15ENSG00000129194
SHBGENSG00000129214
FXR2ENSG00000129245
SAT2ENSG00000141504
ATP1B2ENSG00000129244
WRAP53ENSG00000141499
TP53ENSG00000141510
EFNB3ENSG00000108947
DNAH2ENSG00000183914
RPL29P2ENSG00000240480
KDM6BENSG00000132510
TMEM88ENSG00000167874
CYB5D1ENSG00000182224
CHD3ENSG00000170004
LSMD1ENSG00000183011
CNTROBENSG00000170037
TRAPPC1ENSG00000170043
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:7316543-7316561GGATGGGAGGCAGGAAGC+6.37
RARA(var.2)MA0730.1chr17:7316418-7316435AGGTCACTTGAGGTTCA+6
RFX1MA0509.2chr17:7317070-7317086GGTTGCCATGGTGACT-6.37
RFX1MA0509.2chr17:7317070-7317086GGTTGCCATGGTGACT+6.38
RFX2MA0600.2chr17:7317070-7317086GGTTGCCATGGTGACT-6.48
RFX2MA0600.2chr17:7317070-7317086GGTTGCCATGGTGACT+6.7
RFX5MA0510.2chr17:7317070-7317086GGTTGCCATGGTGACT-6.41
RFX5MA0510.2chr17:7317070-7317086GGTTGCCATGGTGACT+6.53
ZEB1MA0103.3chr17:7317635-7317646CCCACCTGCCC+6.14
ZNF263MA0528.1chr17:7316300-7316321TCCCTTTCTGACCCCTCCTCC-6.06
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1773159597316170
chr1773162717316743
Number: 1             
IDChromosomeStartEnd
GH17I007412chr1773162827317372
Enhancer Sequence
ACACAGGTAG ATTTAAAAAT CCCGCTGCTG CATGTGGTTG CTTATAAGAG GACATTCATG 60
GCCCTGCCCC TCACTAAATG TCCCCACAGC CCTCAAGGCC CCTCAGTCGT TCTCCCAACT 120
AAAATGAAAA AGAAAAGAAA AGAAAAATGT TTAATAATTG GAAAAAAGAA TTATGAAAAC 180
TTCAAACGAA ATTTGAACAA TGTTGGACCC AGTAGAAAAC CTGCCAGAAA AGCTAAACAT 240
GGTGAAAATA AGCTGAAAAA CAAAAAGAAA TTGGAATGTC AGAAAAATAA AATTCAAAAG 300
AATTGGTTAA AATGTTTAGA ATTTGAAAGA AATCTGGACA GTTTTGAAAC TTGTGAAATG 360
TAACATTTGA AAAAACCAAT TTGAAATTGG AACAAAACAA CAGTTCAAAA AAAATTTAAA 420
AGTTGGCAAA TTGATGACAC CATTGAAACA TCAGAAGCCT GTCGCAATTT CCAAAAGCCT 480
GTCAGACACA GAAAACGCAA ACATTCGAAG TGAATTAAAG AATTTGACAA TTTTTTAAAA 540
CAGGGCCCAA TATCTTGAAG TTTCACCACA AAATTTTGAA AAAAAAATGC AAAGAATTTT 600
TTTCTTTTTT TCTTTTTTCC CAAAATGGAT CTTTTTGTTT TTTCTTTTCT TGTTGAATCT 660
GCCCCGAGAG CTTCTTGCTT TTTGGTTGTT TTTTTCTTTC TTTCTTTCTT TCTTCTTTCT 720
TGATCCTGTT TTTGTTGTTG GTTTTGAATT CTTGTCGCCC CAGCCCCTCT TCCTGCTCCT 780
TCCCTTTCTG ACCCCTCCTC CCCTCACACT GGGAGAGGGG TGGGGTGAGG ATGGGAGAAC 840
TGAGGACAAT TAGGACAGGA CCTTGGAGGG AAGGAGATTC CGGCCTGAAA GTGCTGGGAG 900
GTCACTTGAG GTTCAGGAGC AAAGGAGAGG ACAGGATTTG AGGAGAACCC AGCGAGGGTG 960
CTGCCCACAT AGAAGCTCTG GCGGAAGCAG TCAGGAGCAT GGGGGCTGCA CAGGGGGTCT 1020
TAGGGATGGG AGGCAGGAAG CTGTCTGTGA GGTCAAGGAG AATGTCTTAG TGACCTGCAG 1080
GTTGACCTTC TGGCAGGAGG GATGTTTCTA CCAGGATGAG GGAGGTGGGC AGAGATGCTG 1140
GGGACCAGCT GTGGAGGCCC AGGCCTGGCT TTGGTTTGCT GAGTATCCAG GCTAGCAGGG 1200
AGGGCCAGTG TCAAGAAAGA GGAGGGCCTG TGGGCCAGGG GTGACCCCAG CCCTAGCACT 1260
ATGGCTGAAT CATGGGGAGC TGCAGGGGAG GATACTGTAG CCTCGGGGAC CCTGGCAAGC 1320
ACTCTCAGAC TCCCACATCC TCTGGAATTA GTCACCCTTC AGTCCAATCT GGAGCAACTC 1380
AAGGGCCTGA TCACATGTGG CAGTGATCAG GGGATCCTCA GGGGGTATGG CGGGAAGGAG 1440
CCCAGTGCAG AACCCAGGGC TCAGGCCAGT TTGGGGGTGT CCAAAACTAA GCTGCACCCT 1500
GGCTTCATTA AGCAGGCTCT TCCTCCTCCT GCCACAGTAA TTAGGCTGGG GGTTGCCATG 1560
GTGACTGGGG AGGTGACCTA GAAAGGAATT AGGGCGGGGA GGAGACCAAG CCCCAGGGAC 1620
CCTAGGCCTG GCACCCCTCA CCCACAGACC AGGGACCCTA GGCCTGGCAC CCCTCACCCA 1680
CCGACCAGGG TGCCATGTGG AGTGGAGGCC CAAGGCCTGA GTCGGAGGAG ACACCAGGAC 1740
CCTCCCAGCA GCTCCAGCTC CAGTTCTAGC CTCGGGAGCT TGCTCTTCCC AGGGACAGGA 1800
AGGAGATGTG CTGTGTGCGG GGGTGCTGGG GGTTCCCTGG ATCCAGCAGA TGCCCTAAGG 1860
AGGGCCACTG CCCACCCCCA GCCTCTACGG GGTTTCTTGG AAAGTCTGCA TTGGAGAAGT 1920
GCCGCGGGGA AGGCTGGCAG AGGGTGGGGA GGGAATGTCT GCCAGGGCTA GCTGGGGAGG 1980
GAGGAGGGGA ATCCGGTCTT GCCCCCCAGG GATGGGAGTG ACATGTCCCC TGAGCTCCAG 2040
GCCAGTCCTC AGCAGGCCTG GGAGCTGGGC GCTGCTGCTT CCGGTCTGAC TGTGTCCTTG 2100
TCCCTGACCC CCTGGCCCAC CTGCCCACCC CTCCCCACAC 2140