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

TagContent
EnhancerAtlas ID
HS051-05642 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr12:6320420-6323390 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELK4MA0076.2chr12:6320613-6320624GCCGGAAGTGC-6.14
Gata1MA0035.3chr12:6322201-6322212TCCTTATCTGT+6.14
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01613chr12:6320234-6327226Aorta
SE_02955chr12:6320970-6322404Bladder
SE_02955chr12:6322433-6323544Bladder
SE_03308chr12:6320644-6321284Brain_Angular_Gyrus
SE_03308chr12:6322971-6323440Brain_Angular_Gyrus
SE_03988chr12:6320389-6321883Brain_Anterior_Caudate
SE_03988chr12:6322445-6326568Brain_Anterior_Caudate
SE_04905chr12:6320205-6328241Brain_Cingulate_Gyrus
SE_05857chr12:6318642-6328560Brain_Hippocampus_Middle
SE_06790chr12:6318775-6328722Brain_Hippocampus_Middle_150
SE_07876chr12:6320219-6323222Brain_Inferior_Temporal_Lobe
SE_23086chr12:6320271-6323484Colon_Crypt_1
SE_23760chr12:6320424-6321130Colon_Crypt_2
SE_23760chr12:6321189-6322663Colon_Crypt_2
SE_23760chr12:6322715-6323215Colon_Crypt_2
SE_24754chr12:6320348-6321026Colon_Crypt_3
SE_24754chr12:6321035-6323561Colon_Crypt_3
SE_25881chr12:6320552-6321537Duodenum_Smooth_Muscle
SE_26531chr12:6318963-6328738Esophagus
SE_27879chr12:6321701-6322570Fetal_Intestine
SE_30052chr12:6320140-6321734Fetal_Muscle
SE_31631chr12:6320397-6321966Gastric
SE_33937chr12:6322099-6328544HCC1954
SE_35850chr12:6321445-6329804HMEC
SE_37940chr12:6320586-6323707HUVEC
SE_41591chr12:6321199-6322012LNCaP
SE_41591chr12:6322625-6323332LNCaP
SE_42122chr12:6320252-6321143Lung
SE_44470chr12:6320161-6322098NHDF-Ad
SE_44470chr12:6322576-6323518NHDF-Ad
SE_45219chr12:6320083-6322011NHLF
SE_50072chr12:6320199-6326579Sigmoid_Colon
SE_52457chr12:6320397-6322249Small_Intestine
SE_54512chr12:6320070-6346293Stomach_Smooth_Muscle
SE_64246chr12:6320144-6328522NHEK
SE_68793chr12:6320374-6321191H9
SE_68793chr12:6321228-6322414H9
SE_68793chr12:6322557-6326267H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1263224366322600
Number: 2             
IDChromosomeStartEnd
GH12I006211chr1263202566322214
GH12I006213chr1263222806345639
Enhancer Sequence
GTGGAACATA GATAGCAAAT ATTTGAGTAC TTGCTGCTAG TAATTAGGTG ACCTAATATG 60
AAGAAGGAGC TCCTGGCAGA GGGGTAGGGC AGGTTGATAG GTTAGACAAG AGTTTGGGGA 120
TCTTGGCCTC CCTTGCTGGC TTGGGGTTTG CAAGATCCCA TGTTGGAGCA GGAGGGCCGT 180
TCCACCAAGC GGTGCCGGAA GTGCTTTTAG CCGACCCTGC CACTCCAGGC ACCACCTGGC 240
ATTGCTTGAA AACTGTCAAG GAAGGAGCAT CTCCCACCAC TCAGGGCCAC GCACGCACGT 300
GGCGGCCAAC TCTGCAGATG GAATGAGAGC AAGCTGCTGC AAGTGGCTAG AGTGTGTCAG 360
CAAGAGTGTG TGCAGTCATC GCCAGACAGC TCGGCGAGGC ATACACAACG GAAAACAAAT 420
GTGTGGTATT CTGGAATTTA AAGCAAAACA TCCAAAACAA TCCCCCACAT CAGATGATTT 480
TGGTTAAGAT CAGAATGCCT GCTTTCAGTG GAAAAGGGAT TTATGGGCTG GCCAGTGTAT 540
GCTACGCGTC TGGCAAGCAG GCAGTGGAAA CTTGAAATGG GATTTCTTGT TTAGAAAGAG 600
GTTACCTTGG GCTGGGGCCT CCCTCCCAAT CAGCCCCAAC ATCCTAACGC CAGTACACTT 660
CACTGAAGCT TTTCTCCTCT CCAGGGCAGA GGAAGGGCTC CAGGTTTTTA AATGATGCTG 720
ACTTTGTCCT TGAAAGGAGG GAAGATTTCT CAACTCGAAC TTGTTCAGAC CAGGTAGCTG 780
CCTAATTTCC AGAAAGATAT GCTGAGAAAA AGCTTACGGA GTTCCTCATC CTCTGCCACA 840
CCCTGGAGAG GGGACCAAGC TGTCTCCCTT CTATCAGGGA GGAGACAGGT CAGCAAGTAA 900
CCGATCTCTG CATGGCATGT GCTGTGCACC GTCAGAGGAA GAGTGCTGAC AGCTGGGTCA 960
CTCATGCCTG CTCTGTGACC ACGGGCAAGT CGCTTTACCT CTCGGAGCCT GTTTCTTCAT 1020
CTCTCACAGG GATGATTCTA ACTAGCTCTC AGGCTCTAAG GCAGCCCACT AAGAATCAGA 1080
AGGGGCAGCA GGGCCTTGTA GTGTAATTCT AGTCTCCTCC CTGGGAAACC TCTCATGCAT 1140
TGCATTACTG TTGCTCCCAC AGGGAATGTT CTCTTGTAAA GTAATGGCCT GCACCAGCCT 1200
GAGGCCAGGC TCGAACATTT ACACACAACG AGCCAGGCAT AGCAAGGTGG TGGCACCCCC 1260
AGGCTGTAGC TGTCTAGGGC CACCTTCACC CTTCCACCCA GGAGCCCCCC AGCTGCACTA 1320
GCACCCCTGG AAAGGGAGGC CACAGAGTCA GTAGGCAGGC TAAGCATGTG CTTAGGGCAC 1380
CAACAATGCA GGCAGCTCAA GGAATCCAGG GAAATAGGCA CTTTTTTTGA GCTTTATCTT 1440
ACAAGTTCAA CTTTTTTTAT GTTGAATTGT ATGGGTTGTG GGGTAGGTAC CATAATCATC 1500
TCAGTGTCTA GAGCACTAAA TGGCCACAGA AGGCAGAAGT TGGCCTCCCC AGGGACCCAG 1560
CTTGTCATGG AATGTTGGGT TTAAGTGTAT GTGTGGACCC CTCTCCCCAG CCTGCCCTTA 1620
TGGTATAAAA GAGTGACATA TAATAGCAGG GGCCATTTAT GACCCAGGGA CATTGCTGGG 1680
GTTGGGGGGA GTGGGCCAGG AGCGGGCAAG GAGTTGTCTT GATAGAAACG CTGATTCCCG 1740
TGGGGAGACA GCAAATTAGT CACTCTCCTT AAGCCTTACT TTCCTTATCT GTGTAATGAA 1800
GGTAATAACA CAACCAGCGT CTTACGATTG TTACTGGGAC TAAGGGGATA TTTAATGTAA 1860
AGCTATTATA TGGGCCTGGC TCACAGGCAG AGCTTCTGTG TTAGCTTCTG CTGCTGTTGC 1920
TGTAGTTGCT GCTACTGGTA CCTCTCCTTA ACATTTTTCA CAGATTGAGG TTGTCTAAGT 1980
GTTCACATTC ATCCATATCT TCTCACTTCA GTTCATGAAA CCACATCACA CAAGATCAGT 2040
CAATGCTGAA ATTTACCTCC AGTCTTTCTC CCTCTCGAAC ACGAATTGGA GGACGTATCT 2100
TTCCACCTGT CTATAAAACA CTCATTTCTG AGACTTCCCC AGTTTGGGGA AGACGGATAA 2160
AGAAGGGAAT CAGTTTTGCA CTTTGCTGGA AGCGCCTGTA AGAATGCCCC ATTGGCAGAG 2220
ACTCGCTTTG TGGAGCTCAA CTTGGAAATT AATTTACAAT GGAAATTGAA GGAAAATCTA 2280
CTTCATGTCC ACACCAAGAA GGGTGGCCTC AATGCCTCTC CTTCAGTTCA CTCCTTGTGC 2340
CTTCCAAAAG GAAGTTGATT CTTCGTATGT AGAATTTTCT GGACACCTAG AACACCTACA 2400
CCCAGAAACC AGGTCCCAGA GAGATGCAGA GCCACGGTCA CCATTGCTTG TGTAGACACC 2460
AGGGGTAGGA AGTGGAAGGA AGGTAGCGCC TGAGGGTGCA GCTTCCCAGG GACCACCACC 2520
TCTCCCAGCC TCAATGGCGG GAGAGAACAA ACCCAAGGGA GAAGCTACGG GCCAGCATCT 2580
TCCCTCCCTC CCTCTTGGCC CCCACCAGGG CTAGGGTCAA CACCCCAAAT TGAAAGCATC 2640
TGTTGTCAAG CTGCAGCAGG CAGGGAAACC CTGTCACCAG GTTAAGGCTT AAGTCAGAGC 2700
ATTTTGCCAA ATTCAACACG TCCAAGCCTC CCACTTGTCC CCCAAGAAAA TTTCTCAGGG 2760
ATTCACATCT TTCCCAGTCA CCCCCTGGCC AGTGAGGAAG CACCGTGCAT CGAGAAGAGC 2820
ATAGCTTTGA GTCGTCTATG TGGAGCTGGT TCCATCTGAG CTCTGCCTCT TCCTGGCTGT 2880
GTCTTTTTGA GTCAGTTGCT TAAAATCTCT GAGCCTGATT CATCCATAAA ATGAGGGTGA 2940
TGAGAGGATT CAGTGAGAGA CTGTACATAA 2970