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

TagContent
EnhancerAtlas ID
HS088-10245 
Organism
Homo sapiens 
Tissue/cell
HeLa-S3 
Coordinate
chr11:65554940-65556470 
Target genes
Number: 54             
NameEnsembl ID
SYVN1ENSG00000162298
CAPN1ENSG00000014216
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
DPF2ENSG00000133884
TIGD3ENSG00000173825
RP11ENSG00000255478
SLC25A45ENSG00000162241
FRMD8ENSG00000126391
NEAT1ENSG00000245532
MIR612ENSG00000207727
AP000769.1ENSG00000173727
MALAT1ENSG00000251562
SCYL1ENSG00000142186
LTBP3ENSG00000168056
SSSCA1ENSG00000173465
FAM89BENSG00000176973
EHBP1L1ENSG00000173442
KCNK7ENSG00000173338
MAP3K11ENSG00000173327
PCNXL3ENSG00000197136
SIPA1ENSG00000213445
RELAENSG00000173039
KAT5ENSG00000172977
RNASEH2CENSG00000172922
AP001266.1ENSG00000175827
AP5B1ENSG00000254470
OVOL1ENSG00000172818
SNX32ENSG00000172803
MUS81ENSG00000172732
CFL1ENSG00000172757
EFEMP2ENSG00000172638
CTSWENSG00000172543
FIBPENSG00000172500
CCDC85BENSG00000175602
FOSL1ENSG00000175592
C11orf68ENSG00000175573
DRAP1ENSG00000175550
TSGA10IPENSG00000175513
SART1ENSG00000175467
BANF1ENSG00000175334
EIF1ADENSG00000175376
CST6ENSG00000175315
CATSPER1ENSG00000175294
GAL3ST3ENSG00000175229
SF3B2ENSG00000087365
snoU13ENSG00000238752
PACS1ENSG00000175115
KLC2ENSG00000174996
RAB1BENSG00000174903
YIF1AENSG00000174851
RIN1ENSG00000174791
BRMS1ENSG00000174744
B3GNT1ENSG00000174684
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10896045chr1165555524hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr11:65555121-65555132GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:65555898-65555909GGGGGCGGGGC-6.02
KLF5MA0599.1chr11:65555122-65555132GGGGCGGGGC-6.02
KLF5MA0599.1chr11:65555899-65555909GGGGCGGGGC-6.02
MEOX2MA0706.1chr11:65555958-65555968AGTAATTAAC+6.02
SP2MA0516.2chr11:65555896-65555913TTGGGGGCGGGGCGTGG-6.19
ZfxMA0146.2chr11:65555065-65555079GCGGCCGCGGCCTG+7.58
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_24650chr11:65554469-65556603Colon_Crypt_2
SE_24927chr11:65554462-65557521Colon_Crypt_3
SE_27031chr11:65553202-65561915Esophagus
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116555512465556200
chr116555560565556077
Enhancer Sequence
CCAGGTGAGG CTCCAACCGC CCTCCGGCCT GGGGCACCCG CGGCGGCGTC GAGGCTGCGG 60
GCGGGCGGGC GGGCGCAGGT CCGCGGAGCC AGGCGGCAGG CGCGGTGTGG GCGCCGGGGC 120
TGAATGCGGC CGCGGCCTGG GCTGGGTGGG CCCGCGGCTC TCGACCCGGG ACTCGGGGGG 180
CGGGGGCGGG GCCGGCGGAA GAGCGCTGGT CGGGGCGGGG GCTGCATGGT GGAAGGGGAG 240
CCGCTCCCAG GGCCAGGGGG CGCGGAACCG CCTACCCCCA CCCCCTGAAC CGCGGCACAG 300
AGGAGGCAGC GGGGTGTGTC ACCGCTCAGG CGACCCTCGG CTCCGACGTC GTAAATCCAG 360
AAAACCGGGA CTCGCATGAG GCGGGAGAAG GCACTGGAGC GATGCCACTT TGGGGGGCGG 420
GGAGCGGGCT GGAGTTTCGG CCGAGATTTG TGTTAAAAGC TCAGAGCTTC AGCCGCTCGC 480
ACAGGTCCTT CCTCCTCCCC CACAACACTG GTGGCCGGGT CGGAGTGAGG GTCGGGCCGG 540
TGGGGGGCGT GGGCCCCCAA ATTTTCGTTG GGCTCCGGCT GCTAGTCCCG CGCAGTGAGC 600
CGAGACGGTG GGACAGGCGC CCGCTGCGCC CCGCTTGCCC TTAAAGCAGA GGTGGGATCG 660
GGTCTCACCT CTGCTAGAAA CGCACTTCCT TCACCTTGCG GAGGGCACAA TTGCATGGAA 720
AGCAGCTGCA GGGAGCCCAC CCCACAGCGG AGGGCCAGGC CCGGGGAAGC TGGTGTACCC 780
AGTTATTTTT GGCAGACGCC TAGACAGCGT CGACTGTGAG AGTTGCTTCT TCCTCCAGCG 840
GCATCTTCCC CTGAACGCCC CAAGAACACT CCTACCCCTT CTGTCCTCCC CCACCCCCAA 900
CAAAGTCTTT GGTCTGGAGA AAGCCTGCTT CCTTCCGAAC GCCCCCTCCC CAGGCCTTGG 960
GGGCGGGGCG TGGACGCTCT GAACGCCCAG CCCAGCCCCT CCGAGGGGGG AGGGGAGGAG 1020
TAATTAACCA ACTGACTTTG ACCCTTGATC TGCAGACTCC CTGGCACCGC CCCAGGCCTT 1080
GTAGGAAAGT GGGGAAATGA GGGCAGCAGT GAGGGGCCCC GTGAGGGCTC TTGCTCAGTT 1140
TCCCTCCTGA ATAAGCTGTT GGAGACAGTG TCCTGGTGAG GTCTTTGTGG CCTGACCTTC 1200
CAGGACCCAG TGGCCTGTGG CGCTGGCAGG ATGTTTCACA GCTTAACCTG ATCTCAAGGG 1260
GACCCCTCTT CCACCGTTCC TTAAAACAAG GGAATGTGCC AGAAGACCCT GGTAACCCCA 1320
GTGGGGAAAC TGAGGCAAAA AGGGAAGTGA GTGGCCTCCC CACCTGAGGC AGATTAGGGT 1380
GTGGGCTCAG AATTCTGTGT ATAGCTTCTT GCTTGGCCAC ACTCCCTGGT GAGCTGGCTG 1440
GTTCTCTACC TGGGGGTTGG TGGGGGCACG CAGAGGGCCA GAGCCCCCTC CCCGCTCCGC 1500
CCTCCGCCCT CCACCCTCAC CTGTGTTTGA 1530