EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS156-00263 
Organism
Homo sapiens 
Tissue/cell
P493-6 
Coordinate
chr1:27829890-27832120 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:27830565-27830583GGAACGAAAGCAGGAAGA+6.13
Nfe2l2MA0150.2chr1:27831966-27831981TGCTAAGTCATTGTT-6.36
Nr2f6(var.2)MA0728.1chr1:27830156-27830171CGATCTCTTGACCTC-6
STAT1MA0137.3chr1:27831609-27831620TTTCCCAGAAA-6.02
STAT3MA0144.2chr1:27831609-27831620TTTCCCAGAAA-6.32
ZNF263MA0528.1chr1:27831218-27831239TGAGAATGGGGAGGAGGGAGG+6.04
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_02913chr1:27830213-27831026Bladder
SE_02913chr1:27831120-27832355Bladder
SE_05196chr1:27829210-27833352Brain_Cingulate_Gyrus
SE_05814chr1:27829181-27832931Brain_Hippocampus_Middle
SE_06945chr1:27829261-27832857Brain_Hippocampus_Middle_150
SE_07770chr1:27829738-27832662Brain_Inferior_Temporal_Lobe
SE_23188chr1:27830280-27832092Colon_Crypt_1
SE_24033chr1:27830527-27830952Colon_Crypt_2
SE_24033chr1:27830969-27832275Colon_Crypt_2
SE_24711chr1:27830217-27832142Colon_Crypt_3
SE_25901chr1:27830171-27832637Duodenum_Smooth_Muscle
SE_26518chr1:27830129-27832742Esophagus
SE_27625chr1:27830080-27832462Fetal_Intestine
SE_28547chr1:27830055-27832555Fetal_Intestine_Large
SE_29557chr1:27829444-27832772Fetal_Muscle
SE_31394chr1:27830159-27832397Gastric
SE_33477chr1:27830354-27831735H2171
SE_34755chr1:27830079-27832086HeLa
SE_35950chr1:27830256-27832335HMEC
SE_36974chr1:27829579-27833069HSMMtube
SE_39896chr1:27830278-27832548K562
SE_40593chr1:27829483-27832634Left_Ventricle
SE_42106chr1:27830105-27832560Lung
SE_48058chr1:27830093-27832593Psoas_Muscle
SE_48567chr1:27830115-27832554Right_Atrium
SE_50130chr1:27830153-27832341Sigmoid_Colon
SE_51091chr1:27829612-27832640Skeletal_Muscle
SE_52467chr1:27830150-27832427Small_Intestine
SE_62718chr1:27801410-27856116Tonsil
SE_65253chr1:27830186-27832347Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12783030427830805
chr12783080827832117
Number: 1             
IDChromosomeStartEnd
GH01I027502chr12782888927832715
Enhancer Sequence
ACAGAGATAT GTCACAATCA AATGTCCCTT TTGCAGGATC ACTCTGAATT TTTTTTTTTT 60
TTTTTGAGAT GGAGCCTGGC TCTGTTGTCC AGGCTGGAAT GCAGTGGCGC GATCTCGGCT 120
CACTGCAGTC TCCGCCTCCC GGGTTCAAGC AATTCTCCTG CCTCAGCCTT CCAAGTAGCT 180
GGGACTACAG GTGCGCACCA CCACGCCTGG CTAATTTTTG TATTTTTAGT AGAGACGCGG 240
TTTCACCATG TTGGCCAGGA TGATCTCGAT CTCTTGACCT CGTGATCTGC CTGCCTCGGC 300
CTCTCAGAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC CAGCTCACTC TGAATATTTT 360
GAGCGACCTA TTTATGATTT GAATTTATTC ATTCGAGAAG CACCCCAACA TACCTCCTAT 420
ATGTCAGGCA TGGACCCAGG AACTGTGACT ACAACAGATA ATTAGGGGTT GGTTCCTCAG 480
ACAGGACAAA GGGCAGGACA CTGAGTGCCA CCTCTACAGA GGGGTCTGAC TGGATAAAGA 540
CAAAGTGTGA AAGTGTATGA CTTTCACAAA ACAAGAAAGC CAAGCCCCGT GTGGGGTGAC 600
AGGGTGCAGG GATGGGAGAT GGCACTCAGG GAGCTAGCAC TGGACAGGCC AGTGATTCCG 660
AAGACAGAGG ATAAAGGAAC GAAAGCAGGA AGAGAGGGAA TGAGTTATGG GTGAAATATT 720
CGGATCCTGT AGCCTCCATA GAAGGTGGCC AAGTGGGCAG GGGGCAAAGT CCCAGCCAAG 780
CCCCTCAGCA CCCCCATGTG TTCCCAGCCC TGCTGAGCCC TGCAGCTCGT CTCCTCCTGG 840
CTCCAAAAGT CAGACCAAAC CCCGGAGAAC AGAGGCGGGT GAGGAGGGGG CGGTGGGGTA 900
CAAGCCCAGG CCTCTCACCC CAGCAAAGCC TGCCTTCCCA GTGCCTGGGG CCAACCCAGC 960
TGAGAAGCCA GAGGTTACAG GGAAAGGATT AAGGAGTTGC TTGCTTTTTT ACCCAAACTC 1020
TGCTGTATTT CTCTGTCTTT CTTCAATCTC TCTCTCTCTC TCTTTTTTTT TAAAGAAAAA 1080
TATTCCTGTA CACGCACCCA GAGGCTTTTG CAGGAGGCGG CTGTTGGAGA ACTGGGAAAA 1140
CAAGCCAAGA AACAAGAGAG AGGAAAAAGA CCACGCCTCG CCTGGCAGAT TCCTAATGGC 1200
CCAGGAGACC TGAGGCTTTA CAGTGGGAGG CCGGTGGGGG CTGGCTCGGG TGGGAGGGAA 1260
GGGCAGGCCG AAGGACAGCC ACTTGCTGGC TGGTGACCTT GGGCGGGATA CTGCCTGCTT 1320
CCCTCTGGTG AGAATGGGGA GGAGGGAGGC AGGGGCAGGC CTGGCCGGCT GAGGTCACAG 1380
GAAGGCCCCT TCCAGCCTGA AACGCGATCT CGGGATGTGG GGCCTGCCAA CCTGCAGCGA 1440
CCCTGGGCCA GCAGAGATGA AAGGCTGCCT GTCCCCAGCT TCCGGACCCC CAAGGCCCCA 1500
CTGCCTCAAA GTTGGAGAGC AGCAGAGCTG TGTTGCCACT GGCTGGGGCC AGCTGCTGGG 1560
CTCCCCACCC CACCTTATGT CATCCAACCC TCCCTTCCCT GTTTTGCAGA GGACACTCAG 1620
GCCCAGAGAG GGTGGTGACC TGCCTGAGGT CACACAGCAA GCGGGAGTCT GAGCCAAGGC 1680
TCACCACAGT CTTTGGACTC CAAGTCCAGG CCTCCTGCCT TTCCCAGAAA CTTGGCTGCC 1740
TGGGGGCTTA CCCTGGGGAG TTGGAGAGAA CTAGGGCTGG GGAGGACACT TAGGAGCTGT 1800
GTCTGTTTGA AGTCACAACT TAATGTTGAC TAAAGTGCTT TTTTTTTAAA AGACAAAAAG 1860
AAAATTCCCA GCCCCTGCCA TAAGCCTGGA CTTGCTCACT GGCAGGGGAA GGAATGCAGC 1920
TCTGGCCACC ACAGCTGCTG GTGGCCAGCT GCAGCCTCAG CTTCTGCTGC TCCCGCCCCA 1980
GCCGGCAAAG GGACAAAGGC CTCTTCTCAG GCCTGTCCTC TCCAGCCCCC TGGATCAGCT 2040
GGCAGAACAT TGACGGAGCC TCCTCTGTCA CAGACCTGCT AAGTCATTGT TCCTCTCTGG 2100
GCCTTAGTGC CGTTTCTGTA AAATGGGGGC ATAGTATCTG CCTGACCTAC TTCTCAGCAC 2160
TGTTTTGAGG CTCCAAGTAA AGTTCTGGAA ATACAAAGCT CTCAGCGCCT CCTTCCACCT 2220
GCGGGTCTGC 2230