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

TagContent
EnhancerAtlas ID
HS187-03828 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr10:112601030-112604540 
TF binding sites/motifs
Number: 7             
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
RUNX1MA0002.2chr10:112604328-112604339CTCTGTGGTTT+6.14
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: 4             
ChromosomeStartEnd
chr10112601527112602147
chr10112602157112602301
chr10112602586112604280
chr10112602862112603073
Number: 1             
IDChromosomeStartEnd
GH10I110832chr10112592568112607580
Enhancer Sequence
GGATCCAAGC CATCCTCCTG CTTCAGCCTC CCAAATAGCT GGGACTACAG GCATGTGCCA 60
CCACCTCTGG CTAACTTTTT TTTGTAGAGA TAGGGTTTCA CTATGTTGCC CAGGCTAGTT 120
TCAAACTCCT GGGCTCAAGC AATCCACCCA CCTCAGCCTC CCAAAATGTT GGGATTACAG 180
GCATGAACCA TCAAACCTGG CAACAGCAAC TGTTAACTGC CCTCTTAGGC AGTGGTTGGA 240
CATCTGGGCT CAACCCTGTC AACTCCCCAT TCTCTTTTCC CACAATGGCA GTCATATAAA 300
GGTGCCTATC CTGAGTGAAA TTCCAAGCAT GTTGGAGCAG GATGGCCCCA GAGACCCCCA 360
AGCCTCTGCT CTTCCTTTTA CAAGCCAGAA AACAGGCCCA GAGAAGAGAG GTGACTTGTT 420
TGAGGCAACA CAGCTTATTG GTATAGGGCC AAGACTAGAA TCCAGATCCC TTGAGTCTTG 480
CTGGGGCTAC TTGGAGAGTT TATGATATTT CGATTACATT ATCGTGTGAA TTTTCCAGGT 540
CTGGTCCTAG CTGGACTTTG GCACTCAGCA AGGGACTCAA GAGAAATCAT GGATTCTCAT 600
GCTTTGGGTG CATCAGCCGC ACCTGGTGAG CTTGCTAAAA ATGCATATTC CTGGCGCCCC 660
CATGGAGATT CTGACTCATT AGGTCACGGG GAGGACCCAG GCATTTGCAT CTTAGCAAGC 720
CTGGGGGGTA ATTCAATGCA GGTGCAGTCC ACCGATGACA CTTAGAGAAA CACTGCCCTA 780
GATGTCAACC AGGGACTTCC CCAGTAGCTC CTGGAATAGA AGCAGCATTT ATTTTACTGG 840
GTGGTAGGGC CATTGAAGGT AGGGGCACTT TAGTGTGAAA AAGGCTTGAC AGTAGGAGGC 900
AGAGAAAAGG AGACCAGCAT GGCCATGGCA GAAGGGGCTG GTGGCAGCTG GTGGGTGGGG 960
GAGGCGGCGA AGGATGGGGG TGGGAGCGTG TCACAGTCAT CGAACTGGGT TTGGGAGCAT 1020
GTGTTATGAT TTTTAGTTGG GTTCGTACTT ACTGTGCTCA GGCAAAAGTC AATTTTCCAA 1080
TGCTGTCTTT ATCTTTGTTA ATGGCTGGAA GTGTTGTGGT TATTAAACAG CTCCTCGAGA 1140
TCTGATGGAA GCCCTGCTGC TGAAGACAGA GAGCTGTGTG GAGTCAGCAA TCCTTACTCA 1200
GAGGAGAAAC AAGGAACAGG GCCACTGCCC AGGGCCGCGT TGCTGTCAGC GAGGAACTCT 1260
GGGGTCACAC ACACTTTCTC TCCCTCTTCC ACAAGACACT ACTGCTGTCA GCTCGGCCCT 1320
GCTGATTCCT GAGTCCCCCT GCATGGCACA CTTAGTGTAC TCCATAGGGG CACTGTCTCT 1380
TGGCCTCTTC ACAACTGGAG AAGCAGGTAC TGTTATTCTC CCCATTTCAT AGATGGAAAA 1440
TGAGGCTCCG AGAGACAAAG TGGTTTGTCA AGGGTCAGAC GACCAGTAAG TGGCAGAGTT 1500
GGGATTCAAA CCCAGGTCCA CATGACTGTC AAACCACACT CTTAGCCACT ATTCTCCACT 1560
GCCTACCTCC TGTTCCTGCC TCTCCCTAAA GCCTCTAGAC TCTGGGTCTG CCCAGAGCTG 1620
CTTGGATAAA TTAGAAAGTC TAATTTAGCA ATACTGCAGT TACCTATGGC TGAATTCCTG 1680
ATTGTTAAAT TCCAGAAACT GATTTCTCCA GTACCTCTCC TCCCTGGAAA GTAAAGAAAG 1740
GCCTCCACCC ACAGCACTAT ACCCAGAGAA ATACTGTTTC TTCCTTCTTC TCACTTGGGA 1800
GAATATTCCA GGGGAGCTGA GTCTGAGGGC AAGAGAGGAA GGAGGGCCCC GGGGGCTGCT 1860
CAAGTTCCTC CTGTTTCAGG GAGGAGAAGA AAGAGAAGCA GCTTGCTTTC TGCTCTCAGG 1920
GGACTTGGGG ACAAAGGGGA GTGATCAAAA GGGGATTTCC CACAGCCCCA AAATGCTAGC 1980
CGGATTGCAC TTGTGACCTC TCCTTCCTGA GTGAAACTAG ATTGTTGACT TGCCTGCCAC 2040
CTGTTTCCAA CATGGAGTAG AGATGTTGCA CATACATGAT GCCATGTGTC CAGATTAAGA 2100
CAACAAAAAA TTATAAACAA GGATTGAAGA AAGTTGGAGG CAGCAAATAT ATGGTCTGTA 2160
AGGGCTCATA CAGCAAGAGA TGTGACTAGA AGCCTCCTGG GAGCCAAGGC AGAAAGAAAA 2220
AAAAAAAAAA CATGCTCTGT CCTTAGGCTG GAGAGAGCAT TCCAGGTTAT CTGGGGAGAT 2280
TGTTCTACTT GACTCTATAT TCTGGAATAA TTCTCCTGAG GGACAGTACA GAGGTACTGA 2340
GAGGTGTTGG AAAAATCCTT AGGGAGCTCA CAGCCCAACA TTGGAGAAGA GCATAGTGGG 2400
AGCGGGGACA CTGGGATGGC TTCTGGTCTG TGTGAACTGG TTCCTGATGT TGGGGCAACA 2460
CCTCCCAGTG TCCGAAGGCC TGATCCTTGC TCACACCTGC CCAGCCACCT GAGAGTGAGT 2520
ATGCTGGCTG GAGTTCATGA ATTTTTGTTT GGGTTTATTT TCAAGCTCTG TTTTTCAAAT 2580
TTCTCTGTTA AGTGGCTGAA CTTCCAGGAA CCAGTGTTCA CAGGCCAAGG AGGAGGCCAC 2640
CATCATCTCT ACTACCTGAG TGCCCTGCCA CACCCACCTG ACAATAGAGA GCTCTAGGGT 2700
GGGGCCCCTG CTCTTTGGAT TGTTGGGGGA AATAAACCTC TCCAGCATTT ATTCTTTGGG 2760
GTTACCCCAA ACGGATGACC ACAGCCAGGA GGGAACAAAG CCTGACTGGG AAGTGCTGAT 2820
TCTCTCTGGC AGTTTGGGAA CTTCCCCTCA AACCTGTCTG ATAAGGAGCG GCCTAGGGAG 2880
GAGGGGTGCA AAAGGTGTGC CCCGTTTGCC CGTGAGATCT CTCACCATCA CTGTATGCAA 2940
GCCTAGGAAG AACAGAGCTT TCTGGCTCAG GGACAGATCT CCATGCTGGG AATCAGGACC 3000
TTGAGTTCCT GGGTCAAATC CACAATGAAC TCATTCTGAG ATGTAGGCAA ATGTTTACCT 3060
TCTGTTGCTT CGGTTTTCCC ATCTGTGCAT TTGATGTGTG CCTTGTGCGT GCCAGAGGTT 3120
TTTGGGAAGA AAATAAGAGT GGAGACTTGC TGTCAATCAC AAGGTGGGGG GTGGTCACTT 3180
CTCTACCTGA ATCTCCCACA TGGGCCTGTG GGGAGCTATG GTCCTTATTA CCATCCTCCT 3240
GCCCCCAGCA GGGGAGCCTA CCCATGAGGC AGGCTTGCTT GGGGTCGGCC AGCCTGGTCT 3300
CTGTGGTTTT TGTCTCCTGG GCTCCTCGTA TGGCTTAGCT TGGCCCTCCA CCGACCCTAC 3360
TTAATCTTGC CTCCTCTCCA CCCACCTTCT CACCCCCACA GCCTCCATTT GTGGTTCAGC 3420
TATGCTCAGT GCCTCGGGGG TTCCCAAATA GGCCCCTTCC AGCTCCTTGA TTTTGTAAAT 3480
GGTTTTCCCA CTGCTAGGAA TACCTTTTGG 3510