EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-04683 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr10:112601300-112604240 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:112602858-112602876GCAAGAGAGGAAGGAGGG+6.09
FOSMA0476.1chr10:112601699-112601710TCTGACTCATT+6.32
RARAMA0729.1chr10:112603012-112603030GATTGCACTTGTGACCTC-6.01
RELMA0101.1chr10:112602980-112602990GGGGATTTCC+6.02
RREB1MA0073.1chr10:112601971-112601991TGGCAGCTGGTGGGTGGGGG-6.3
ZNF263MA0528.1chr10:112602909-112602930GGAGGAGAAGAAAGAGAAGCA+6.07
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_09857chr10:112602026-112603976CD14
SE_20267chr10:112601065-112604084CD56
SE_23151chr10:112599888-112604756Colon_Crypt_1
SE_24035chr10:112601641-112604747Colon_Crypt_2
SE_25029chr10:112599914-112604792Colon_Crypt_3
SE_25873chr10:112599164-112601864Duodenum_Smooth_Muscle
SE_25873chr10:112601935-112607502Duodenum_Smooth_Muscle
SE_26657chr10:112599961-112604755Esophagus
SE_27704chr10:112595240-112607543Fetal_Intestine
SE_28632chr10:112593028-112607614Fetal_Intestine_Large
SE_31444chr10:112599873-112604809Gastric
SE_32525chr10:112600632-112604717GM12878
SE_33439chr10:112601572-112608225H2171
SE_43605chr10:112600001-112606555MM1S
SE_47589chr10:112602055-112603069Pancreas
SE_47589chr10:112603246-112604762Pancreas
SE_50110chr10:112599883-112607504Sigmoid_Colon
SE_52404chr10:112599892-112604830Small_Intestine
SE_58452chr10:112593100-112642895Ly1
SE_59745chr10:112593531-112634215Ly4
SE_60671chr10:112600128-112635801DHL6
SE_60982chr10:112552689-112654127HBL1
SE_61666chr10:112600053-112634910Toledo
SE_62307chr10:112592977-112644561Tonsil
SE_67012chr10:112601572-112608225H2171
SE_67382chr10:112600001-112606555MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr10112601527112602147
chr10112602157112602301
chr10112602862112603073
Number: 1             
IDChromosomeStartEnd
GH10I110832chr10112592568112607580
Enhancer Sequence
TCTCTTTTCC CACAATGGCA GTCATATAAA GGTGCCTATC CTGAGTGAAA TTCCAAGCAT 60
GTTGGAGCAG GATGGCCCCA GAGACCCCCA AGCCTCTGCT CTTCCTTTTA CAAGCCAGAA 120
AACAGGCCCA GAGAAGAGAG GTGACTTGTT TGAGGCAACA CAGCTTATTG GTATAGGGCC 180
AAGACTAGAA TCCAGATCCC TTGAGTCTTG CTGGGGCTAC TTGGAGAGTT TATGATATTT 240
CGATTACATT ATCGTGTGAA TTTTCCAGGT CTGGTCCTAG CTGGACTTTG GCACTCAGCA 300
AGGGACTCAA GAGAAATCAT GGATTCTCAT GCTTTGGGTG CATCAGCCGC ACCTGGTGAG 360
CTTGCTAAAA ATGCATATTC CTGGCGCCCC CATGGAGATT CTGACTCATT AGGTCACGGG 420
GAGGACCCAG GCATTTGCAT CTTAGCAAGC CTGGGGGGTA ATTCAATGCA GGTGCAGTCC 480
ACCGATGACA CTTAGAGAAA CACTGCCCTA GATGTCAACC AGGGACTTCC CCAGTAGCTC 540
CTGGAATAGA AGCAGCATTT ATTTTACTGG GTGGTAGGGC CATTGAAGGT AGGGGCACTT 600
TAGTGTGAAA AAGGCTTGAC AGTAGGAGGC AGAGAAAAGG AGACCAGCAT GGCCATGGCA 660
GAAGGGGCTG GTGGCAGCTG GTGGGTGGGG GAGGCGGCGA AGGATGGGGG TGGGAGCGTG 720
TCACAGTCAT CGAACTGGGT TTGGGAGCAT GTGTTATGAT TTTTAGTTGG GTTCGTACTT 780
ACTGTGCTCA GGCAAAAGTC AATTTTCCAA TGCTGTCTTT ATCTTTGTTA ATGGCTGGAA 840
GTGTTGTGGT TATTAAACAG CTCCTCGAGA TCTGATGGAA GCCCTGCTGC TGAAGACAGA 900
GAGCTGTGTG GAGTCAGCAA TCCTTACTCA GAGGAGAAAC AAGGAACAGG GCCACTGCCC 960
AGGGCCGCGT TGCTGTCAGC GAGGAACTCT GGGGTCACAC ACACTTTCTC TCCCTCTTCC 1020
ACAAGACACT ACTGCTGTCA GCTCGGCCCT GCTGATTCCT GAGTCCCCCT GCATGGCACA 1080
CTTAGTGTAC TCCATAGGGG CACTGTCTCT TGGCCTCTTC ACAACTGGAG AAGCAGGTAC 1140
TGTTATTCTC CCCATTTCAT AGATGGAAAA TGAGGCTCCG AGAGACAAAG TGGTTTGTCA 1200
AGGGTCAGAC GACCAGTAAG TGGCAGAGTT GGGATTCAAA CCCAGGTCCA CATGACTGTC 1260
AAACCACACT CTTAGCCACT ATTCTCCACT GCCTACCTCC TGTTCCTGCC TCTCCCTAAA 1320
GCCTCTAGAC TCTGGGTCTG CCCAGAGCTG CTTGGATAAA TTAGAAAGTC TAATTTAGCA 1380
ATACTGCAGT TACCTATGGC TGAATTCCTG ATTGTTAAAT TCCAGAAACT GATTTCTCCA 1440
GTACCTCTCC TCCCTGGAAA GTAAAGAAAG GCCTCCACCC ACAGCACTAT ACCCAGAGAA 1500
ATACTGTTTC TTCCTTCTTC TCACTTGGGA GAATATTCCA GGGGAGCTGA GTCTGAGGGC 1560
AAGAGAGGAA GGAGGGCCCC GGGGGCTGCT CAAGTTCCTC CTGTTTCAGG GAGGAGAAGA 1620
AAGAGAAGCA GCTTGCTTTC TGCTCTCAGG GGACTTGGGG ACAAAGGGGA GTGATCAAAA 1680
GGGGATTTCC CACAGCCCCA AAATGCTAGC CGGATTGCAC TTGTGACCTC TCCTTCCTGA 1740
GTGAAACTAG ATTGTTGACT TGCCTGCCAC CTGTTTCCAA CATGGAGTAG AGATGTTGCA 1800
CATACATGAT GCCATGTGTC CAGATTAAGA CAACAAAAAA TTATAAACAA GGATTGAAGA 1860
AAGTTGGAGG CAGCAAATAT ATGGTCTGTA AGGGCTCATA CAGCAAGAGA TGTGACTAGA 1920
AGCCTCCTGG GAGCCAAGGC AGAAAGAAAA AAAAAAAAAA CATGCTCTGT CCTTAGGCTG 1980
GAGAGAGCAT TCCAGGTTAT CTGGGGAGAT TGTTCTACTT GACTCTATAT TCTGGAATAA 2040
TTCTCCTGAG GGACAGTACA GAGGTACTGA GAGGTGTTGG AAAAATCCTT AGGGAGCTCA 2100
CAGCCCAACA TTGGAGAAGA GCATAGTGGG AGCGGGGACA CTGGGATGGC TTCTGGTCTG 2160
TGTGAACTGG TTCCTGATGT TGGGGCAACA CCTCCCAGTG TCCGAAGGCC TGATCCTTGC 2220
TCACACCTGC CCAGCCACCT GAGAGTGAGT ATGCTGGCTG GAGTTCATGA ATTTTTGTTT 2280
GGGTTTATTT TCAAGCTCTG TTTTTCAAAT TTCTCTGTTA AGTGGCTGAA CTTCCAGGAA 2340
CCAGTGTTCA CAGGCCAAGG AGGAGGCCAC CATCATCTCT ACTACCTGAG TGCCCTGCCA 2400
CACCCACCTG ACAATAGAGA GCTCTAGGGT GGGGCCCCTG CTCTTTGGAT TGTTGGGGGA 2460
AATAAACCTC TCCAGCATTT ATTCTTTGGG GTTACCCCAA ACGGATGACC ACAGCCAGGA 2520
GGGAACAAAG CCTGACTGGG AAGTGCTGAT TCTCTCTGGC AGTTTGGGAA CTTCCCCTCA 2580
AACCTGTCTG ATAAGGAGCG GCCTAGGGAG GAGGGGTGCA AAAGGTGTGC CCCGTTTGCC 2640
CGTGAGATCT CTCACCATCA CTGTATGCAA GCCTAGGAAG AACAGAGCTT TCTGGCTCAG 2700
GGACAGATCT CCATGCTGGG AATCAGGACC TTGAGTTCCT GGGTCAAATC CACAATGAAC 2760
TCATTCTGAG ATGTAGGCAA ATGTTTACCT TCTGTTGCTT CGGTTTTCCC ATCTGTGCAT 2820
TTGATGTGTG CCTTGTGCGT GCCAGAGGTT TTTGGGAAGA AAATAAGAGT GGAGACTTGC 2880
TGTCAATCAC AAGGTGGGGG GTGGTCACTT CTCTACCTGA ATCTCCCACA TGGGCCTGTG 2940