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

TagContent
EnhancerAtlas ID
HS101-08103 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr11:66631430-66633540 
Target genes
Number: 55             
NameEnsembl ID
PACS1ENSG00000175115
KLC2ENSG00000174996
RAB1BENSG00000174903
RP11ENSG00000254452
CNIH2ENSG00000174871
YIF1AENSG00000174851
RIN1ENSG00000174791
BRMS1ENSG00000174744
B3GNT1ENSG00000174684
SLC29A2ENSG00000174669
MRPL11ENSG00000174547
PELI3ENSG00000174516
DPP3ENSG00000254986
CTDENSG00000255517
BBS1ENSG00000174483
ZDHHC24ENSG00000174165
CCSENSG00000173992
CCDC87ENSG00000182791
RBM14ENSG00000239306
RBM4ENSG00000173933
RBM4BENSG00000173914
SPTBN2ENSG00000173898
C11orf80ENSG00000173715
RCE1ENSG00000173653
LRFN4ENSG00000173621
PCENSG00000173599
C11orf86ENSG00000173237
SYT12ENSG00000173227
RHODENSG00000173156
KDM2AENSG00000173120
AP001885.1ENSG00000179038
ADRBK1ENSG00000173020
ANKRD13DENSG00000172932
SSH3ENSG00000172830
POLD4ENSG00000175482
7SKENSG00000201684
AP003419.11ENSG00000256514
CLCF1ENSG00000175505
RAD9AENSG00000172613
TBC1D10CENSG00000175463
CARNS1ENSG00000172508
PPP1CAENSG00000172531
RPS6KB2ENSG00000175634
AP003419.16ENSG00000255949
PTPRCAPENSG00000213402
CORO1BENSG00000172725
TMEM134ENSG00000172663
AIPENSG00000110711
PITPNM1ENSG00000110697
CDK2AP2ENSG00000167797
DOC2GPENSG00000231793
NUDT8ENSG00000167799
TBX10ENSG00000167800
RPL37P2ENSG00000239559
FAM86C2PENSG00000160172
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:66631994-66632012CCATGCTCCCTTCCTTTC-6.27
SNAI2MA0745.2chr11:66632252-66632262TGCACCTGTT-6.02
ZNF263MA0528.1chr11:66632029-66632050AAGGGAGGATGGGAGGGAGAG+6.18
ZNF263MA0528.1chr11:66632057-66632078CGAGGAGGAAGTGGGAGAGGA+6.52
ZNF263MA0528.1chr11:66632032-66632053GGAGGATGGGAGGGAGAGGAG+6.94
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_24585chr11:66630878-66632731Colon_Crypt_2
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr116663146766631559
chr116663283466633068
chr116663214166632247
Number: 2             
IDChromosomeStartEnd
GH11I066864chr116663210166632250
GH11I066865chr116663227466635318
Enhancer Sequence
TGGGAAGGGT GAGGCGTGAG GACCTGCGCC AGAAACTGCG GTCAAAAGTG CCCCACCCAC 60
CCCGAGGCTG GCCAGGTGTG CACCCAGCAG CTGCTGAGAG CAGAGCGTGG GGTGTCTGCA 120
GGTGAATCCC AGCTCTGGCT GGTCAGGTTT TGCTGTTTCT GCCACCAAAC CCAGGAGTGC 180
GTCCCTTCTC TACGTGCCAC GCAGTCACTG CTACTGGCTC CCTGTGAGGA GCTGGGAGGG 240
GGCAGAGGAG GAAGGGAATG CCTGCCGCAG AGCGGGAGAG GGGCCCGGGC AGGCAGGGGC 300
CAGCCCTGCC TCTATTCCCA CGGACCTGCT GCACCTGCCT GAGCAACCCT CTAGCCTTTC 360
AGACTCATCC ACGTTCGTTC CACAGCACGG ATTGAGGTCT GCTGACCCGG CCGCTAAAGG 420
GCCTCGCCGT GGGCTCCCAG ACAGCGAGGG GACGGCAGGC CGGCGACAGG GCCTCCAAAG 480
GACCATGTGC GAGGCAAGAG GCAAGGCTGA CCGGGGGTTT GTTTTTGTTT TTAACAGGGT 540
GGTGGGGAAG GCCTCAACAT CCACCCATGC TCCCTTCCTT TCCTTTCCTT TCCTTCCAGA 600
AGGGAGGATG GGAGGGAGAG GAGGCAACGA GGAGGAAGTG GGAGAGGAAA TGAAGGGAAA 660
GTGCCAGAGG CAGGGTCCAC ACCCATCAGG GAAGCAAACC AAGGGCGAGG AGAGGGCAGC 720
GGGGCAGCGG GACAGGGCCA GGGCCAGACG GCAATGGGAG GGGCAGCGGA GAGGAGGAGA 780
CAGAGGCGCC GACACTCACA CACACAGGTG GCTCGTGCCG CCTGCACCTG TTCGTGCCGC 840
CCGAGTGAGC CCCGCAGAGA AGGGCTCCCC GGAGGTGGGG GACCCGTCAG GCCCAGGTAA 900
GGAAGAAGGG GAGTGGGGGG ACCGCCCAGA GGGGCTCGGG ACACCCACTG CCCATTTCCG 960
CTTCTCGGGG GCAGAGGCCT GTGTTCAATA AAAAGGAACT TCATAAAATA TTTAAGGGTG 1020
AACACTCAGC TGAGAGCAGA AACTGTCGGC TAAAAATACT CTGTGATGAG GCAGGCTCTG 1080
AAGAGCCAGG GCTTGGAAGT GGGGATGGAG GGAGGCAGAG AAGTCAGGGG CCGCCGGGCA 1140
GCACTCAGCC TGGGGCTGCC GCCACCTACA GACTCTTCCA GAAACAGAAG GCAGGTGGCC 1200
AGCTCCCTGC TGAAGCCACA GGCTCTGCTG CTTCCAGAAT CCAGAGAGCT CTGGTCCCTA 1260
CCCCCAGCCT CCCCAGCCTC CCTTGTCTCA GAAGCCCAGA GCCTGGCCCA AACTCATGTT 1320
TGCTCCCCTC ACCGCCCCAC ACAAGCCCGG GGGCCTCTGC CTTGGACTCT GGAGCAAAGC 1380
TGGAGCTCCA TCAATGTCTT GCCTCCTTTG GGGCTCAGGC CCCTGGATAG GGAGCAAGTC 1440
CCTAGCACAG CTGGCACGGT GCTGGCAGCA CGTGCAGGGC TGGGAACAGG CACCGAGCAG 1500
GCCGCAGGGC TCCTGCCCAC AGCTGGGACC AGAGGCGGGG GAGATGGGTT TCGGAGGCCA 1560
ATGACTGGGT CCCGGTGCTG AGAGGAAGAA AGGTACAGGG AGCCCTCCTG GAGAAGGCGC 1620
GAGTCTTGCT GTGCTGAGGA GCCTGCCGTG GACCGCCTCA GCGCCCCCTA CACCACTCTC 1680
TCCCCCACCA AGGCTGCCAT CTCGCGGCCC CGAATCTACC TCTCGGTCTC CCTCCTGTGC 1740
CGCCATCTCC GACTCCCTCC CCCATCCTTG ATGGGCCCCT GAGCTTGGCT CAGACTCCAT 1800
TGGGACCTCT GGGCCCAGTC CTTTGCCACC CCCACCCCCA GGTCCTGCCA TGTCAGCCCA 1860
TCCCTCAGAT GGGAGGTGGT GCTTGGGCTC CGTCGGCAGC CAGGCGTGGG GCTCCTGTGG 1920
GAGCTGGAGG GTCAGGGGCT GGCTTTGTGT CTGGGTCCCT GCGTTTTGCT CCACCAAGCC 1980
AGCCTGCTCC CCGCTCCCAC CCTCACGGCT TCCTCCTGAC CTGGGCGCCC AGCAGTCTCT 2040
TCCCCTGGGA GGCGCCGCCC CTCCTCTGGG CACTGCCTGC CTCCGTGTAC TCTATGTCCA 2100
CTTCAGAGCC 2110