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

TagContent
EnhancerAtlas ID
HS051-27813 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr9:130677120-130678680 
Target genes
Number: 39             
NameEnsembl ID
FAM129BENSG00000136830
STXBP1ENSG00000136854
C9orf117ENSG00000160401
RP11ENSG00000248666
TTC16ENSG00000167094
PTRH1ENSG00000187024
TOR2AENSG00000160404
SH2D3CENSG00000095370
CDK9ENSG00000136807
FPGSENSG00000136877
YENSG00000222421
RN5S296ENSG00000222455
ENGENSG00000106991
AK1ENSG00000106992
ST6GALNAC6ENSG00000160408
ST6GALNAC4ENSG00000136840
PIP5KL1ENSG00000167103
DPM2ENSG00000136908
FAM102AENSG00000167106
SLC25A25ENSG00000148339
NAIF1ENSG00000171169
AL590708.2ENSG00000232850
PTGES2ENSG00000148334
LCN2ENSG00000148346
C9orf16ENSG00000171159
DNM1ENSG00000106976
CIZ1ENSG00000148337
MIR199BENSG00000207581
AL590708.1ENSG00000221297
SWI5ENSG00000175854
GOLGA2ENSG00000167110
COQ4ENSG00000167113
TRUB2ENSG00000167112
SLC27A4ENSG00000167114
TMSB4XP4ENSG00000223551
URM1ENSG00000167118
ODF2ENSG00000136811
GLE1ENSG00000119392
SPTAN1ENSG00000197694
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SREBF1MA0595.1chr9:130678151-130678161ATCACCCCAC+6.02
ZEB1MA0103.3chr9:130678156-130678167CCCACCTGCCC+6.14
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_10486chr9:130677004-130681316CD19_Primary
SE_11194chr9:130676247-130682355CD20
SE_17726chr9:130676842-130681077CD4p_CD25-_CD45RAp_Naive
SE_20250chr9:130677079-130679316CD56
SE_21396chr9:130677586-130679760CD8_Memory_7pool
SE_23690chr9:130676786-130679297Colon_Crypt_1
SE_44595chr9:130678207-130679396NHDF-Ad
SE_47725chr9:130677470-130679328Pancreas
SE_50413chr9:130676589-130682381Sigmoid_Colon
SE_53230chr9:130676827-130680013Small_Intestine
SE_59014chr9:130662884-130684756Ly3
SE_62503chr9:130658860-130684719Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9130677400130678000
Enhancer Sequence
CTGAGGGAGA CAGTGGCCAT GGGGGGGTGT ATGTGGGGAG GGGCTCCCAG AAGCCCCTTC 60
AGCGCTGCAC CTGGCCTCCT GGGTCTAGAG AAGCTCCTGG GTCTAGAGCA GCTCCTAGAA 120
CAGCAGCAGA ATCCAGTCTC CATCCACTGG GCCTTACCTG GGGATGCCAA GCTCTGGGCA 180
CATAAGGCCC CGGAGATAAC ACTGTTATCA TCCCCACATT CTAGATAAGG AAAGCAGTTT 240
GGAGTGAAGT GTGTAGTACA AGGCCATACA GCAAAGAAGC AGCACAGTGG GGCCTTAAAT 300
ACTGGCTGGA AAGCCCATAT TCCTAACTGG AGGCTAGGGT GTACTGTGCG ACCTATGGCT 360
CTCCATCCCT CTGGGCCTGT TTCCTCCTCT ACAAACTGGG GACTGATAAT GCCCACCGTG 420
TGAACTTACG GGAGGGGGGC AGTGAAAGCC TTCTGTATAC TGTAAAGTGC TGTGCACATG 480
ACAACGGGAA AGTGGTGCCT CAGAAGGGCC ACCAGCCCCT TCAGCCTAGG ACCAGGGCTG 540
CCTAGTGTGG CCCCGCCTCC TCCCCACCCC CAGCTGACTC AGTGGCTGTC CCCTGGTGAT 600
CCGGATCTGG GTCAGCAGGC CAGGTGGCAC AAGGAGATTG GAGCAAAGGT CACTCAAGAA 660
ATGGTTTTAA TAATTGAAAA GCTGGTGCCT GGAGGCTACC GCCTCCAGAA ACCATGTGCC 720
AAAGGCCATT GGAACCAGGA AGCTCTTCTA GCCATCTGGC CTAGACCCAG CCTGGGGCTG 780
GTCCTGCTGG CAGACTTAGT GAATGCCCCT ACCACCACCA AGCCTCCCAG GAGGGGAAGG 840
GCTTGGTGGC AGCAGAACTG TGGGCTAGTC ACTGGGTAGT GGGCCACCCT GGTCACCACG 900
TGTGTCTCTC TGGGCTCCAG GTTTCTAGAC TCGAGGCACA AGTCCCTAGG CCACCCTTCA 960
GAAGCCACCA AGCAGTTGGC TGGTGCTCTC CAAAAATCAG AAGTGGGAAA GTGGCCCCCA 1020
CCCCCTACCC CATCACCCCA CCTGCCCCGG CGCATCCTGC CTGAGGCCCA CCATTTTCTG 1080
CCCGCAAGCT ACGTCAGCTT CTAAAAATAA GTCTTTTCTG TGTGGCCAGC TGTGCAGGGG 1140
AGGGAGTTCT GCCTGGCACC TGCTCCCCTG CCCATGAGGA ACCAGAGACC TTGACTCAGG 1200
CAGTCGAGAT GAACTGCCCC CCACATCCAG CTCTCTCTCT CACAGCCCGG GGCTTCTGCA 1260
GTAAAGACAA GAGCGGCTGA ACTGAACTTC ACAACCCCAG TTCCACGTAG GCTTTGCCTG 1320
GTGAGCTCGT AGCGTTACCT CCGTTTTACA GGGATAGCAA GGTACTGACA CTGCAGAGTG 1380
GATGCCACCT GCCTGGGGCC ACACGGTCTG CAAGAACAGG GTTGGACTTT GAGGCCATTC 1440
TGCCCTTCTC TGCTCAGCAG TAGGGAGGTC AGAAGTGGCA GTGGGTCCTG GGGTGGAGAG 1500
GCTGCTGAGC TGCTCCGCCA GTCGGGGCCT CTGCGTTCCC TGGAAGTCCT CCTTCTTCCC 1560