EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS161-15780 
Organism
Homo sapiens 
Tissue/cell
PC3 
Coordinate
chr9:137263280-137266140 
Target genes
Number: 6             
NameEnsembl ID
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
LMX1BMA0703.2chr9:137265679-137265690ATTTTAATTAA+6.62
SPI1MA0080.4chr9:137263955-137263969TACTTCCCCATTTA-6.03
SPICMA0687.1chr9:137263955-137263969TACTTCCCCATTTA-6.55
Sox3MA0514.1chr9:137265662-137265672CCTTTGTTTT+6.02
YY1MA0095.2chr9:137263697-137263709CAAGATGGCTGC+6.74
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00174chr9:137261148-137271210Adipose_Nuclei
SE_00860chr9:137261032-137275300Adrenal_Gland
SE_02933chr9:137262940-137265682Bladder
SE_02933chr9:137265704-137267801Bladder
SE_05812chr9:137261360-137282798Brain_Hippocampus_Middle
SE_09174chr9:137254160-137271835CD14
SE_23121chr9:137264346-137265593Colon_Crypt_1
SE_23757chr9:137264349-137265626Colon_Crypt_2
SE_24707chr9:137263084-137265478Colon_Crypt_3
SE_24707chr9:137265846-137266565Colon_Crypt_3
SE_26524chr9:137261081-137273486Esophagus
SE_31436chr9:137263056-137265664Gastric
SE_33498chr9:137264862-137274948H2171
SE_34906chr9:137261183-137274052HeLa
SE_40986chr9:137262434-137273204Left_Ventricle
SE_41556chr9:137243649-137273607LNCaP
SE_42130chr9:137261389-137273101Lung
SE_43440chr9:137261193-137264159MCF-7
SE_43440chr9:137265603-137267722MCF-7
SE_48050chr9:137252285-137278501Psoas_Muscle
SE_49423chr9:137262969-137272077Right_Atrium
SE_50152chr9:137263044-137271792Sigmoid_Colon
SE_51460chr9:137262103-137271156Skeletal_Muscle
SE_52424chr9:137265772-137271780Small_Intestine
SE_53315chr9:137260801-137271867Spleen
SE_54834chr9:137263825-137271890Stomach_Smooth_Muscle
SE_65247chr9:137261076-137277919Pancreatic_islets
SE_68695chr9:137265176-137266584H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9137263305137264168
chr9137264339137265222
chr9137264490137265116
chr9137265242137265562
Number: 1             
IDChromosomeStartEnd
GH09I134369chr9137261189137279971
Enhancer Sequence
GGCTGCCGTG TGTCCAGCGA GAGCCAGCTG GGCTGAGCTT CTCCTCAAAT GCTGATGGGG 60
GCCAGACTTC TGGGGGCACC GTCTCTTTCC ATAACATGAT CTCCCCTAGG CCTCGCCCCT 120
AACAAGCTGG CAGAGAACTC TCGCCCCATT TCATGGCCAT GGCACTGGTG GCTTGGGGCA 180
GGGCCTGGCG GCCAGCTCTT GGGCCGGTGC CTCTGGTTCA CTGGGCCTGT GGCCTGGCCC 240
TTGGGGTATG GAGGACGGGC CTGGGGGTGG CGTGCGCCCC CTTGAAGTGG TCCGCCCTTG 300
TCTCTGCCTG TCCTGAGGAT GAGGGTCATC AACTGAGTCG GGGCCACAGG GCAGCCATGG 360
GTGCGCGAGT GCAGGGCCGG GCCTGTCTCC TCCGGGCGGC GTGGCAGGTG GCTGGGCCAA 420
GATGGCTGCA GCGCTTCCTG GGCGCTGCTG CGTGTTGAAA CCCGTCTGTG ACGTGGCCAG 480
CGGTGTTGAA ATAAGTGCCT GTGCATTTCC CAACATCCTG CCAGCCTGGT GCAGGACTGG 540
GTGCCAGGCC CAGCCTGGGC CTCCCTTGTG GGGTGCTCAG GCCCCACTTC CCTCCCTGGG 600
GAGGGGAGGA GAGGCCACCT CGAGGGAGTG ACGTCAAGGC AGGGTGACAT TAGTCTGGGC 660
CCACGGGATC CTTGCTACTT CCCCATTTAT GGAGGGGAAA CTGAGGTGTG GAGAGGGGTG 720
AGGATGGGTT TGAAGCCCGG CCATCCAGTC TCAGTGCCGC TTGTAGAGGC AGAAGGGCGT 780
AGGGAGGGAG AGGGAGAGCC AGGTAGGCCG AAGGCGCCTG GCAGTGTGGC AGGACACGCG 840
CCCACTGGGG AGGTGGAGGG CCGCAGCCAG GGCCTCAGCT GAGGGCCTCC TGGATGCTGG 900
CTTTGCTGTT GGGGCTGGAG CATGGACCCG TCCTGGGCCG ATTATGGGAG ATGGTGTGGA 960
GTGGGGGCCG CAGGCGAGGG TCCCTCTTCC TTTGGCTGGA GGAGGCCTGG CCCTGGGACT 1020
GTCCCGTGAG GGGAGACAGT GGTTGGACCC ATTGCAGAAT TGATTTGTTA TCACTGGGTT 1080
CCAGGCACAC GGCTTAGAGG GCATCACGGA GGCCTCCCCG TCACCTCAGA GGGCATCACG 1140
GAGGCCTCCC CATCATCTTA TGGGGTGGGT GTTATTAGGC TTAGTTTAGA GGAGACAGAG 1200
GATCAGAGAG GCCCACTGAC CCGCCTTGGG GCCCCCAGCA GGCAGAGGAA CTGTGTCCAG 1260
GTGCTGGACT GTGAGACCCT GCTCTTCCCG GGACTCTACC ACCTCAGAGG GTGGCAGCAC 1320
AGGGCCCAGC AGGGCGTGTG CTCCTGTGGG GCAGGCGAGT CCTGGCTCTG CCCTTGTAGG 1380
CTGTGTGACC CCAGGCGGTA GCTCAGGCTC TCTGGTCTGG ACTGGGCGCG GAGCTGCTTG 1440
AGATCTGGAA TCTGGCTTTC TGGTGAAGGG GCAGCAGGAG AGGGGCTGAG ACCCAGCCTT 1500
CCTGGTTGCA GAGCTGCGGT AGGCCAGACC CTCCTGCCTG CTGGGTGGGG CCTGGCATTC 1560
CAGGAACCTG TGGTCAAGCC TGGCCTGGGC TGTGGCGTCT GCCCCGGGTT CGTCAGCAGG 1620
GGAGGGGCCC TGGAGACCAG TCCGTTATGG ATGAGGAAGC GGGTGCCCAG AGAGGGTGAG 1680
GAGCTGGGCT GGGCCACACA GCCAAGTGGC CACAGAGCTG GGGGTGGTCA GGAGCCATGC 1740
TTTCTGGTAA GGCGGAAGTG TCTGGGGCCC GGGTGGGATG AAGGACTCGG GTCCCAGAGA 1800
CCAGCCTTTG GTGCTGTTCT TGGGCTAGGA ATGGCAGTAA CAGGAAGGGC ATGGCCACCG 1860
AGACGCACTG AGTTATGGGC ACCTGCCGTC TGCCAGGAAC TGTGGTCCAC GCCCGACTGT 1920
CTTTAACAGC TCTGTGCCTG CTGCTGTGTG CCGGGCCCTG CGCTCAGCCC TTCTCGTGTG 1980
TGGTCTCCAA CCCTGTGTTT TCCCAGGCCG TTGGCCCATT TTCCAGATGA GAATACTGCG 2040
GCCCAGAGAA GCAGCATTGT GTGCTGCGGT CCTTGGCCAC GAGGTGGTGT GGGTTTTTTT 2100
GACCCAGATC TTCCTGTCTA TCACCCTCCC TGGGCCTACC TTCCTTATGG TAGACACATG 2160
TGCAGGTCTG TCCCATCCCC CAGCTATCCA CAGAGAGGCC AGGGTTTGGC ATGGGGAGGT 2220
GTCGGAGCCT ACTGGGTTGT AGCTGGAGGG AGGTGAGTGG CACCTCCCAC AGGAAGCCCC 2280
CCTTGATGTC TCCTCCACCT TGCCACATTA CCAGCCGATA GCCAGGTTCC TGGAAAAGGC 2340
TGTCTTTCTG ACTCTGGACT GGGTGCCCCT GGGCAGGGCC CACCTTTGTT TTCTAATTTA 2400
TTTTAATTAA AAATTTAAAA ATTAGAGACA GAGTCTTGCT TTGTTGCCCA GGCTAGACGT 2460
GAACTCCTGG GCTCAAGTGA TCCTCCCGCC CCGGCCTCTC GGGTAGTGGG GACTTCAGGA 2520
GTGCGCCACC TCACCTGGCC TCCCAGCCTG GTTTTTCTCT GCCTGTTTGT AGCCCTGGGT 2580
TCGACGGGGG AAGCAGTCGC CTGATGGGCA AGTGCTCTCT GAGTGGTGCA TGAAGGTGGC 2640
TGTCCACGTG GCTGTCTGTG GTGTCGGTTA ATCGTCACGG CTTCCGGGAG TTAAAGGTGA 2700
GGGTGCCATC CCCTTTCTGG GGACAAGGAC GTTTAGAACC AGCGAGGTTG AGTCAGATGC 2760
CCAAGGCCCT ACCCAGCCGA GAGCGATGCA GCCAGGACTC AAACCCAGAT CCGCAGGCGG 2820
CGGCCGCTGT GCCCCAGTGG AGCTTGAGCC TGGGTGGTGG 2860