EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS104-01101 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr1:27830420-27833320 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:27830565-27830583GGAACGAAAGCAGGAAGA+6.13
Nfe2l2MA0150.2chr1:27831966-27831981TGCTAAGTCATTGTT-6.36
STAT1MA0137.3chr1:27831609-27831620TTTCCCAGAAA-6.02
STAT3MA0144.2chr1:27831609-27831620TTTCCCAGAAA-6.32
ZNF263MA0528.1chr1:27831218-27831239TGAGAATGGGGAGGAGGGAGG+6.04
Number of super-enhancer constituents: 31             
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_26518chr1:27832803-27834041Esophagus
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: 1             
ChromosomeStartEnd
chr12783080827832117
Number: 2             
IDChromosomeStartEnd
GH01I027502chr12782888927832715
GH01I027506chr12783280427834041
Enhancer Sequence
TGGATAAAGA CAAAGTGTGA AAGTGTATGA CTTTCACAAA ACAAGAAAGC CAAGCCCCGT 60
GTGGGGTGAC AGGGTGCAGG GATGGGAGAT GGCACTCAGG GAGCTAGCAC TGGACAGGCC 120
AGTGATTCCG AAGACAGAGG ATAAAGGAAC GAAAGCAGGA AGAGAGGGAA TGAGTTATGG 180
GTGAAATATT CGGATCCTGT AGCCTCCATA GAAGGTGGCC AAGTGGGCAG GGGGCAAAGT 240
CCCAGCCAAG CCCCTCAGCA CCCCCATGTG TTCCCAGCCC TGCTGAGCCC TGCAGCTCGT 300
CTCCTCCTGG CTCCAAAAGT CAGACCAAAC CCCGGAGAAC AGAGGCGGGT GAGGAGGGGG 360
CGGTGGGGTA CAAGCCCAGG CCTCTCACCC CAGCAAAGCC TGCCTTCCCA GTGCCTGGGG 420
CCAACCCAGC TGAGAAGCCA GAGGTTACAG GGAAAGGATT AAGGAGTTGC TTGCTTTTTT 480
ACCCAAACTC TGCTGTATTT CTCTGTCTTT CTTCAATCTC TCTCTCTCTC TCTTTTTTTT 540
TAAAGAAAAA TATTCCTGTA CACGCACCCA GAGGCTTTTG CAGGAGGCGG CTGTTGGAGA 600
ACTGGGAAAA CAAGCCAAGA AACAAGAGAG AGGAAAAAGA CCACGCCTCG CCTGGCAGAT 660
TCCTAATGGC CCAGGAGACC TGAGGCTTTA CAGTGGGAGG CCGGTGGGGG CTGGCTCGGG 720
TGGGAGGGAA GGGCAGGCCG AAGGACAGCC ACTTGCTGGC TGGTGACCTT GGGCGGGATA 780
CTGCCTGCTT CCCTCTGGTG AGAATGGGGA GGAGGGAGGC AGGGGCAGGC CTGGCCGGCT 840
GAGGTCACAG GAAGGCCCCT TCCAGCCTGA AACGCGATCT CGGGATGTGG GGCCTGCCAA 900
CCTGCAGCGA CCCTGGGCCA GCAGAGATGA AAGGCTGCCT GTCCCCAGCT TCCGGACCCC 960
CAAGGCCCCA CTGCCTCAAA GTTGGAGAGC AGCAGAGCTG TGTTGCCACT GGCTGGGGCC 1020
AGCTGCTGGG CTCCCCACCC CACCTTATGT CATCCAACCC TCCCTTCCCT GTTTTGCAGA 1080
GGACACTCAG GCCCAGAGAG GGTGGTGACC TGCCTGAGGT CACACAGCAA GCGGGAGTCT 1140
GAGCCAAGGC TCACCACAGT CTTTGGACTC CAAGTCCAGG CCTCCTGCCT TTCCCAGAAA 1200
CTTGGCTGCC TGGGGGCTTA CCCTGGGGAG TTGGAGAGAA CTAGGGCTGG GGAGGACACT 1260
TAGGAGCTGT GTCTGTTTGA AGTCACAACT TAATGTTGAC TAAAGTGCTT TTTTTTTAAA 1320
AGACAAAAAG AAAATTCCCA GCCCCTGCCA TAAGCCTGGA CTTGCTCACT GGCAGGGGAA 1380
GGAATGCAGC TCTGGCCACC ACAGCTGCTG GTGGCCAGCT GCAGCCTCAG CTTCTGCTGC 1440
TCCCGCCCCA GCCGGCAAAG GGACAAAGGC CTCTTCTCAG GCCTGTCCTC TCCAGCCCCC 1500
TGGATCAGCT GGCAGAACAT TGACGGAGCC TCCTCTGTCA CAGACCTGCT AAGTCATTGT 1560
TCCTCTCTGG GCCTTAGTGC CGTTTCTGTA AAATGGGGGC ATAGTATCTG CCTGACCTAC 1620
TTCTCAGCAC TGTTTTGAGG CTCCAAGTAA AGTTCTGGAA ATACAAAGCT CTCAGCGCCT 1680
CCTTCCACCT GCGGGTCTGC CTTCTCACTG TGCCCTTTGC CTCGACCACC CCTCCCTCCC 1740
TCATGCTTTC CCTGGCCAGC CCCAACTCAC TCAGCTCAGC TCAGTGGGAC CATCACCTGC 1800
TCTAAAACCT GCCCTCAACT TCTGAAGGAG GCACCTTCAG AAGAAAAAAG ACGGCAGTGC 1860
TGTATTTATC ATGGTTGTAC ATAATTAAAT AATTGGCCAG TGTGGTGCCT CAGGCCTGTA 1920
ATCCCAACAC TTTGGGAGGC TGAGGTGGGA GGATTACTTG AAGCCAGGTG TTCAAGACCA 1980
GCCTGGGCAA CATGGCAAAA CCCTGTCTCT ACAAAAAATA AATTAGCTGG GCATGGTGGC 2040
ATGTGCCTGT AGTCCCTGCT ACTCGGGAGG CTGAGGTGGT AGGATGGATT GAGCCTGGGA 2100
GGTTGAGGAG TGACCTGCAG TGAGCTGTAA CTGTGCCACT GAACTCCAGC CTGGGTGACG 2160
GAGTGAGGCC CTGTCTCAAA CATAAAAATA AAAATAAATT AAATAGGTCA GGGGTGGCGG 2220
TGGCTCACAC CTGTAATCCC AGCACTTTGG GAGGCTGAGG CAGACAGATC ACCTGAGGCC 2280
AGGAGTTTGA GACCAGCCTG GCCAAAATGG TGAAACCCCG TCTCTACTAA AAGTACAAAA 2340
ATTAGCCAGG CATGGTGGCA CACGCCTGTA GTCTCAGCTA CTCAGGAGGC TGAGGCAGGA 2400
GAGTCGCTTG AATCCAGGAG ACGGAGTTTG CAGTGAGCCA AGATCGCGCC ACTGCACTCT 2460
AGCCTGGGCA ACAGAGCAAG ACTCCGTCTC AATAATAATA ATAATGAATT AAATAATTAA 2520
TTGTGCAATT GGATCCTCGT TAAAATGTAA ACTCTAATAA TAGCTAATGT CAAATGCTGA 2580
CCCGGGGCCC AGGACTTTAC ATTTAACCCA TTTAATCTGC ATGGTAGGTA CTGTTGGTAT 2640
CGCCATCTTA CAGATGAAGA AACAGACAAT GAGAGGTTCA CTCACTCACC TGAAGTCACA 2700
GCAAGTTGGA GGCTGAGCCA GGACTCACCA CAAATAAGTT GCAAATCAGG ATTCAAATGC 2760
AGACCGCCGG CTATAACCAT TACATCACTA ATGACACGGG TTTAGTTTGT GCCCTGATGT 2820
ATCCCCGGTT CCCGGCACAG CATCTGGCAT ACAGCAGGTG CTCCATATAT GTTAGATAAA 2880
TACATACACA AATAGGTGAT 2900