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

TagContent
EnhancerAtlas ID
HS105-17393 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr12:6319540-6322230 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELK4MA0076.2chr12:6320613-6320624GCCGGAAGTGC-6.14
Gata1MA0035.3chr12:6322201-6322212TCCTTATCTGT+6.14
Klf1MA0493.1chr12:6319566-6319577AGGGTGTGGCT-6.02
Nr2f6(var.2)MA0728.1chr12:6320222-6320237TGAACTCCTGACCTT-6.04
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_01613chr12:6319028-6319991Aorta
SE_01613chr12:6320234-6327226Aorta
SE_02955chr12:6320970-6322404Bladder
SE_03308chr12:6320644-6321284Brain_Angular_Gyrus
SE_03988chr12:6318969-6320195Brain_Anterior_Caudate
SE_03988chr12:6320389-6321883Brain_Anterior_Caudate
SE_04905chr12:6320205-6328241Brain_Cingulate_Gyrus
SE_05857chr12:6318642-6328560Brain_Hippocampus_Middle
SE_06790chr12:6318775-6328722Brain_Hippocampus_Middle_150
SE_07876chr12:6318312-6319855Brain_Inferior_Temporal_Lobe
SE_07876chr12:6320219-6323222Brain_Inferior_Temporal_Lobe
SE_23086chr12:6319050-6320172Colon_Crypt_1
SE_23086chr12:6320271-6323484Colon_Crypt_1
SE_23760chr12:6319095-6319874Colon_Crypt_2
SE_23760chr12:6320424-6321130Colon_Crypt_2
SE_23760chr12:6321189-6322663Colon_Crypt_2
SE_24754chr12:6319060-6320180Colon_Crypt_3
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_31631chr12:6319037-6319856Gastric
SE_31631chr12:6320397-6321966Gastric
SE_35850chr12:6321445-6329804HMEC
SE_37940chr12:6320586-6323707HUVEC
SE_41013chr12:6319009-6319932Left_Ventricle
SE_41591chr12:6321199-6322012LNCaP
SE_42122chr12:6319058-6320063Lung
SE_42122chr12:6320252-6321143Lung
SE_44470chr12:6320161-6322098NHDF-Ad
SE_45219chr12:6320083-6322011NHLF
SE_48662chr12:6319028-6320067Right_Atrium
SE_50072chr12:6319030-6320121Sigmoid_Colon
SE_50072chr12:6320199-6326579Sigmoid_Colon
SE_52457chr12:6319049-6320051Small_Intestine
SE_52457chr12:6320397-6322249Small_Intestine
SE_54512chr12:6318102-6320065Stomach_Smooth_Muscle
SE_54512chr12:6320070-6346293Stomach_Smooth_Muscle
SE_64246chr12:6320144-6328522NHEK
SE_68793chr12:6319031-6319995H9
SE_68793chr12:6320374-6321191H9
SE_68793chr12:6321228-6322414H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1263198106319999
Number: 2             
IDChromosomeStartEnd
GH12I006210chr1263191386320069
GH12I006211chr1263202566322214
Enhancer Sequence
CCCTGACTAT ATGACCAGTG GAACCAAGGG TGTGGCTGAA GCTCTCAGGA CAAAGGCCAG 60
GGAGAGGAAG CACCGGCTGT TTTTTTTAGA CTCTCTTCGA GCACCCACTA CCCCCACTGC 120
CCCCAAGCGA GGCCAGGTGT AGGTGGCATC TCCAGCCCAG GTGGCCATGC AGCTGCCCTG 180
CTGTCAGGGA GGAGGCGCGT CTGCAAGCTG CCTTCCTTCC GGTGCAGATG GGCTCCCTTG 240
TGGCCTTTAA AGATCGAAAA CACCACTTTG AAATGGGATT AGATATGAAT GGGGGGGAAA 300
CAGGCAAAAG GGAAAAAATT CTGGCTTCAG AATAGAAGAA ATGGATCAAA AACACAAACA 360
GCTTAACAAA ATAATTGAGA ATTGGGGCTC TGCAGTCAGA CCATTCTGGG TTCAAGTTCT 420
AACTCTGCCA CTTACTTGCC CTGTGATCTC AGTTGAGCAA CTTTTTTTTT TTTTTTTTTT 480
TGAGAAGGAG TCTCGCTCTG TTGCCAGGCT GGAGTGCAGT GGCGTGGTCT TGGGTCACTG 540
CAACCTCTGC CTCCTGGGTT CAAGCGATTG AACAGCCTCA GCCTCCCAAG TAGCTGGGAT 600
TACAGGCACG CACCACCATG CCTGGCTATT TTTTTATATT TTTAGTAGAG ATGGGGTTTC 660
ACCATGTTGG CCAGGCTGGT CTTGAACTCC TGACCTTGTG ATCCTCCCGC CTTGGCCTCC 720
CAAAGTGCTG GGATTACAGG CTTGAGCCAC CGTGCCCGGC CCGAGCAACT TAACTTTTGT 780
GCCCCAGTTT TTTCATCTAA AAAATAGAAG ACAATATTAC CTCTTTGGTG GGCCTATTCT 840
GAAAACTAAA TAGTTCTGGA GAAGTGCTTA GGGTGGGGTT GTGGAACATA GATAGCAAAT 900
ATTTGAGTAC TTGCTGCTAG TAATTAGGTG ACCTAATATG AAGAAGGAGC TCCTGGCAGA 960
GGGGTAGGGC AGGTTGATAG GTTAGACAAG AGTTTGGGGA TCTTGGCCTC CCTTGCTGGC 1020
TTGGGGTTTG CAAGATCCCA TGTTGGAGCA GGAGGGCCGT TCCACCAAGC GGTGCCGGAA 1080
GTGCTTTTAG CCGACCCTGC CACTCCAGGC ACCACCTGGC ATTGCTTGAA AACTGTCAAG 1140
GAAGGAGCAT CTCCCACCAC TCAGGGCCAC GCACGCACGT GGCGGCCAAC TCTGCAGATG 1200
GAATGAGAGC AAGCTGCTGC AAGTGGCTAG AGTGTGTCAG CAAGAGTGTG TGCAGTCATC 1260
GCCAGACAGC TCGGCGAGGC ATACACAACG GAAAACAAAT GTGTGGTATT CTGGAATTTA 1320
AAGCAAAACA TCCAAAACAA TCCCCCACAT CAGATGATTT TGGTTAAGAT CAGAATGCCT 1380
GCTTTCAGTG GAAAAGGGAT TTATGGGCTG GCCAGTGTAT GCTACGCGTC TGGCAAGCAG 1440
GCAGTGGAAA CTTGAAATGG GATTTCTTGT TTAGAAAGAG GTTACCTTGG GCTGGGGCCT 1500
CCCTCCCAAT CAGCCCCAAC ATCCTAACGC CAGTACACTT CACTGAAGCT TTTCTCCTCT 1560
CCAGGGCAGA GGAAGGGCTC CAGGTTTTTA AATGATGCTG ACTTTGTCCT TGAAAGGAGG 1620
GAAGATTTCT CAACTCGAAC TTGTTCAGAC CAGGTAGCTG CCTAATTTCC AGAAAGATAT 1680
GCTGAGAAAA AGCTTACGGA GTTCCTCATC CTCTGCCACA CCCTGGAGAG GGGACCAAGC 1740
TGTCTCCCTT CTATCAGGGA GGAGACAGGT CAGCAAGTAA CCGATCTCTG CATGGCATGT 1800
GCTGTGCACC GTCAGAGGAA GAGTGCTGAC AGCTGGGTCA CTCATGCCTG CTCTGTGACC 1860
ACGGGCAAGT CGCTTTACCT CTCGGAGCCT GTTTCTTCAT CTCTCACAGG GATGATTCTA 1920
ACTAGCTCTC AGGCTCTAAG GCAGCCCACT AAGAATCAGA AGGGGCAGCA GGGCCTTGTA 1980
GTGTAATTCT AGTCTCCTCC CTGGGAAACC TCTCATGCAT TGCATTACTG TTGCTCCCAC 2040
AGGGAATGTT CTCTTGTAAA GTAATGGCCT GCACCAGCCT GAGGCCAGGC TCGAACATTT 2100
ACACACAACG AGCCAGGCAT AGCAAGGTGG TGGCACCCCC AGGCTGTAGC TGTCTAGGGC 2160
CACCTTCACC CTTCCACCCA GGAGCCCCCC AGCTGCACTA GCACCCCTGG AAAGGGAGGC 2220
CACAGAGTCA GTAGGCAGGC TAAGCATGTG CTTAGGGCAC CAACAATGCA GGCAGCTCAA 2280
GGAATCCAGG GAAATAGGCA CTTTTTTTGA GCTTTATCTT ACAAGTTCAA CTTTTTTTAT 2340
GTTGAATTGT ATGGGTTGTG GGGTAGGTAC CATAATCATC TCAGTGTCTA GAGCACTAAA 2400
TGGCCACAGA AGGCAGAAGT TGGCCTCCCC AGGGACCCAG CTTGTCATGG AATGTTGGGT 2460
TTAAGTGTAT GTGTGGACCC CTCTCCCCAG CCTGCCCTTA TGGTATAAAA GAGTGACATA 2520
TAATAGCAGG GGCCATTTAT GACCCAGGGA CATTGCTGGG GTTGGGGGGA GTGGGCCAGG 2580
AGCGGGCAAG GAGTTGTCTT GATAGAAACG CTGATTCCCG TGGGGAGACA GCAAATTAGT 2640
CACTCTCCTT AAGCCTTACT TTCCTTATCT GTGTAATGAA GGTAATAACA 2690