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

TagContent
EnhancerAtlas ID
HS108-41580 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr9:130871540-130873440 
Target genes
Number: 44             
NameEnsembl ID
SNORA65ENSG00000201302
RPL12ENSG00000197958
FAM129BENSG00000136830
STXBP1ENSG00000136854
C9orf117ENSG00000160401
RP11ENSG00000248666
TTC16ENSG00000167094
PTRH1ENSG00000187024
TOR2AENSG00000160404
SH2D3CENSG00000095370
CDK9ENSG00000136807
FPGSENSG00000136877
ENGENSG00000106991
AK1ENSG00000106992
ST6GALNAC6ENSG00000160408
ST6GALNAC4ENSG00000136840
PIP5KL1ENSG00000167103
DPM2ENSG00000136908
FAM102AENSG00000167106
SLC25A25ENSG00000148339
NAIF1ENSG00000171169
AL590708.2ENSG00000232850
PTGES2ENSG00000148334
LCN2ENSG00000148346
C9orf16ENSG00000171159
DNM1ENSG00000106976
CIZ1ENSG00000148337
SWI5ENSG00000175854
GOLGA2ENSG00000167110
COQ4ENSG00000167113
TRUB2ENSG00000167112
SLC27A4ENSG00000167114
TMSB4XP4ENSG00000223551
URM1ENSG00000167118
MIR219ENSG00000207955
CERCAMENSG00000167123
ODF2ENSG00000136811
GLE1ENSG00000119392
SPTAN1ENSG00000197694
WDR34ENSG00000119333
SETENSG00000119335
PKN3ENSG00000160447
ZDHHC12ENSG00000160446
snoU13ENSG00000239055
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELK4MA0076.2chr9:130871749-130871760GCCGGAAGTGC-6.14
IRF1MA0050.2chr9:130872855-130872876AAAAAAAAACAGAAACAAAAA-6.6
ZBTB7AMA0750.2chr9:130871748-130871761CGCCGGAAGTGCC+6.34
Number of super-enhancer constituents: 18             
IDCoordinateTissue/cell
SE_23076chr9:130869595-130872622Colon_Crypt_1
SE_23076chr9:130872815-130874357Colon_Crypt_1
SE_23771chr9:130871488-130872399Colon_Crypt_2
SE_23771chr9:130873016-130873691Colon_Crypt_2
SE_24841chr9:130871075-130872008Colon_Crypt_3
SE_24841chr9:130872718-130873868Colon_Crypt_3
SE_25948chr9:130871324-130872562Duodenum_Smooth_Muscle
SE_25948chr9:130872806-130873871Duodenum_Smooth_Muscle
SE_27710chr9:130871299-130872696Fetal_Intestine
SE_27710chr9:130872752-130873797Fetal_Intestine
SE_28658chr9:130871270-130872686Fetal_Intestine_Large
SE_28658chr9:130872700-130873803Fetal_Intestine_Large
SE_29715chr9:130871701-130872555Fetal_Muscle
SE_29715chr9:130873061-130873705Fetal_Muscle
SE_31462chr9:130871451-130872611Gastric
SE_31462chr9:130872905-130873732Gastric
SE_48196chr9:130867631-130874420Psoas_Muscle
SE_51250chr9:130867549-130874463Skeletal_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9130871826130872200
Number: 1             
IDChromosomeStartEnd
GH09I128110chr9130871532130873717
Enhancer Sequence
TTTCTGACGG GGGCCTGGGT GGTCTGGGGG TGCTGACATG TTAGAAAATG CGCCCTGTTT 60
TCCCCTCTGG AGCCTGGTGG TGCCCCCTTT CGGCTTCTTA GAGGCGCTCC CTCTTTAATG 120
GTTGCGTGTT CGATTTGGGG TGCCCTGAGT TGCTGTGTAG GGTCGTTCCT CAGCCTGTCT 180
CAGGCAGGGT GCGGGGGATC TCTCCCTCCG CCGGAAGTGC CATCTTCACA GACACCGAGG 240
ACGTCGCTGG GCTTCTCTCC CCTCCCCCCA GCTGCCCCTC CCAGCCTCAC CCCGCTCCTG 300
CCTCCTCACA CCCTCTCAGT AACCTCATCT GACTGAGGAT TACCTTCAAT ATCTATATTT 360
AGATGACACT CCTTTGATAC TTGAACGAAT TCCAGCTTCA TCAGTACAAC TGTGAAATCC 420
ACATCCACTT AAACAGCACC TCGAGTTCAG CATGTCAGAA GCCGAACCCT TCATTTTCCT 480
CCCAAAATCT GCTTCTTCAT TTTCCTCATG CCAGCAAATG GCAACTCCTT TCTTCTACGA 540
ACTTAAGCCA AACACCTTGT AGTCAACCTG ACTCTGTACT TCCCTCTGGT TCCAGGGCAG 600
TCCACCAGCA AATACCGTCA GCCCCACCCG CAAAATAGAT CTGCTCTCTG GCCGCTTCTC 660
CCGACCTCCA CCCCTGCCAC TGATCAAAGA CAATATCATG TCTCACCTGG ATGATTGCAA 720
GACCTAAACT TCTTCCCCCT GCTTCCCTTC ACTCTCCACC CCAAGACCAA GGGGCCCTTT 780
GAAAACCTAA GTGGATAGCC AGGTGTGATG ACAGGTGCCT ATAATCCCAG CTACTCCAGA 840
GGCTGAGGCA GGAGAATGGC TTGAACCCAG GAGGCAGAGG TTGTGGTGAG CCGAGATCAT 900
GCCACTGCAC TCCAGCCTGG GCGACAGAGT AAGACTCTGT CTCAAAAAAA GAAAACCTAA 960
GTTTCTCATG TCACTCAGAT CCTCCAATGA ATAGATAAGC TGGGCAGGCG CGGTGGCTCA 1020
CGCCTGTAAT CCCAGCACTT TGGGAGACCG AGGTGGGCGG ATCACCTGAG GTCAGGAGTT 1080
TAAGACCAGC CTGGCCAACA TGGCAAAACC CCATCTCTAC TAAAAATACA AAAATTAGCT 1140
GTGCTTGGTG GCGCATGCCT GTAATCCCAG CTACTCGGGA GGCTGAGACA GGACAATCAC 1200
GTGAACCCGG GAGGCAGTGG TTTCAGTGAG CTGAGATCAT GCCACTGCAC TCCAGCCTGG 1260
GCGATAGAGC GAGGAGACTC CATCTCAGAA AAAAAGAAAA GAAAAAAAAA GAAAAAAAAA 1320
AAAACAGAAA CAAAAACGAA AAAGACAAGT CACCGGCTAG GAGAAAATCT TTGCAGTACA 1380
TGTAATCTCC AGCATGTATT AACTGTGTAA GGCAAAAAGA AGAGGACAAG CCAGTTAACA 1440
ATTGGCACTT CCAAAAGCAA GATGACTTAA TGGCCAATAA ACATGAAAAC GAGCTTAACT 1500
CCATTAGTTG TCAGGGAGAA GCAAAACACT GAATGAGGCC CAGAGCAGTG GCTCACACCT 1560
GTAATCCCAG CACTTCGGGA GGGTGAGGCT GGAGATCACT TGAGGCCAGG TGTTCAAGAC 1620
CAGACTATGC AATACAGCAA GGCCCCATCT CTACCAAAAC AGTTAAAAGC ATTTAACAAG 1680
ATACCAGTGC ATCCACACTA GAAGGCCTAG AACTAAAGAT GTCAGCACTG TAGTTTGATG 1740
AGAATCTGGG AGCAGCCACA CTCCTAGACT CTGCTAGTAC AAGGTAAAAT GCCAATCATT 1800
TTGGAGAATT GTTTCTAATA AACTCAAATG GACATTTGCC CTGTGACCCA GCACTTCCAC 1860
TCCTATTTAC CCCTTTCCCT AAATGAAAAC ATCCACAGAA 1900