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

TagContent
EnhancerAtlas ID
HS101-11625 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr12:123353110-123355430 
Target genes
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2AMA0052.3chr12:123355270-123355282TCTAAAAATAAA+6.07
RREB1MA0073.1chr12:123353445-123353465CCGCCAACCACCACCCCCCA+7.4
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01099chr12:123351803-123353378Adrenal_Gland
SE_01099chr12:123354616-123355337Adrenal_Gland
SE_03969chr12:123355116-123358789Brain_Anterior_Caudate
SE_04866chr12:123348693-123353944Brain_Cingulate_Gyrus
SE_04866chr12:123354237-123359304Brain_Cingulate_Gyrus
SE_05835chr12:123351481-123359219Brain_Hippocampus_Middle
SE_06752chr12:123351674-123353530Brain_Hippocampus_Middle_150
SE_06752chr12:123354724-123358851Brain_Hippocampus_Middle_150
SE_07820chr12:123351569-123353711Brain_Inferior_Temporal_Lobe
SE_07820chr12:123354601-123359255Brain_Inferior_Temporal_Lobe
SE_11355chr12:123352410-123359477CD20
SE_12882chr12:123354940-123357018CD34_Primary_RO01480
SE_13364chr12:123352751-123353355CD34_Primary_RO01536
SE_23035chr12:123354594-123357509CD8_primiary
SE_23125chr12:123351854-123353484Colon_Crypt_1
SE_25026chr12:123351443-123353773Colon_Crypt_3
SE_26757chr12:123351797-123353344Esophagus
SE_26757chr12:123354675-123358275Esophagus
SE_28186chr12:123355056-123357781Fetal_Intestine
SE_29262chr12:123355173-123357938Fetal_Intestine_Large
SE_30119chr12:123355056-123358608Fetal_Muscle
SE_31427chr12:123343773-123359126Gastric
SE_37349chr12:123351755-123353831HSMMtube
SE_37349chr12:123354568-123359385HSMMtube
SE_40937chr12:123349311-123353958Left_Ventricle
SE_40937chr12:123354579-123358546Left_Ventricle
SE_41807chr12:123354586-123355141LNCaP
SE_42306chr12:123344180-123353834Lung
SE_42306chr12:123354685-123359130Lung
SE_47190chr12:123350856-123362813Panc1
SE_47585chr12:123352084-123353401Pancreas
SE_47585chr12:123355016-123355370Pancreas
SE_49030chr12:123349908-123353426Right_Atrium
SE_50159chr12:123351960-123353568Sigmoid_Colon
SE_52477chr12:123351884-123353646Small_Intestine
SE_53586chr12:123351577-123353480Spleen
SE_61538chr12:123340041-123395084Toledo
SE_62830chr12:123354785-123387061Tonsil
SE_64309chr12:123351846-123353606NHEK
SE_65302chr12:123349486-123353585Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12123354936123354986
Number: 1             
IDChromosomeStartEnd
GH12I122866chr12123350977123353655
Enhancer Sequence
TGGAAAAAAA GCAAGAGGTA TGACAAAAGT GAGAGGTGTC CAGGTAAAGC CCTTCATGAT 60
GCCAACCACG GCAGGATTGC ACCTTCCTTT CCAGGAAGCT GAATGTGAAA GGCTTGAAAA 120
CCTACAGGGG AACAAGTGCA CCAAGCCAGT GCCCAGGGGC CAACATCCCA TGTCAGAGCA 180
ACCTGTGTCA CCAGCTGCTT CTAGAACCAG CTGTTTTCAA ATATGGGGCA GTGACATTCT 240
CATCATGCCA CTTTGTATTT CCTTTATGTT TTGAGTGGTA ACTTACATCG AGTATACACA 300
TCTCAAGTGT GTAAGTCAAA TTTCCACGTG TTTAACCGCC AACCACCACC CCCCAGATCC 360
AGACACAGAA CCTTTCCACC GGGCGCCCTC ACGCCCACTG CACCCGCCAG ATAACCCCTA 420
CGCTGGCCTC CACCACCACA GAGGAGGTCC GCCTGGTCTT GACTCCACAT CCTGGAATCA 480
GAGAGTACAG GTCATACTCT CCTGGCTTCT TGCACTCAGC ACCGCGTCTC TGAGACCCTG 540
CTCAGGTCTG TGAATCAGTT CGTTTCTTTC CAATGCTGTG TAGTGTTCCA TTGTGTAAAC 600
AGACTTTATG TGCCCATCAC TCTGTAGACG GACATTTTTA TTGTTTCCAA ATTTTATTAT 660
AAGGTAATAA AGATACAACA TTCTTGTACC TATCTTCTGA GAGACATTAA TATCCACTTC 720
TGTTGGGTAT ACACCCAGGA GCAGAGCTGC TGTGCAGCGC ATACACACTC TTCATTCTAG 780
CAGGTGCTAC CCAACAGCCT TCCCCAGGTG AAATGAGAAA AGGAGGTGGC TGTGGCAGTG 840
CAGCCTGCAA GCCCCAGATG ACCCATGGAC ACTCCTACCA GCAAGATGCA CGGCACCTCA 900
CAGCACTTGG TACTGCCAGT CTTTTTACTT TTCGTCATTC TGGTTTGGGT GTATGATCGT 960
AAATTTTTAC TGAAGTTAAT GGAGAAAATG ACAAGATGAT AGCAAGTAGT GACAGACATC 1020
ACTGTAAACC TCACTGCAGA AGGTGATCTT TAACCCAAAC TCTTTAAAGG GATGGGGTCT 1080
CTGTCACCCA GGGTGGAGTA CAGTAATGCA ATCACAGTTC ACTGTGGCCT CAGCCTTCAG 1140
AGTAGGTGGG ACTATAGGCG AGCACCACCA CCCCCAGCTT ATTTCACTTC TTTTGTAGAG 1200
ACACAGTCTC GCTCTGTCGC CCAGGCTGGA GTACAGGGCT GCAATCATGG CTCACTGCAG 1260
CTTCAATCTC CAAGGCTCAA GCAATCCTCC TTCCTTAGCC TCCCAAGTAG CTAGGACCAT 1320
AGGCGTGTGC CACCACCCCC AGCTCTGACT TTATCTAAAT GTCCCTTTGA TAACTATCAA 1380
AAGCACTTAG GATGCTCAAC AATCTTTAAT TCTGATGTCT CCTCCTAATG GCTGCAAATT 1440
AAAGTATGCC ATTAAAATAA AGTGTTTCAG TGATGCTTTT TTTTTTTTTT TTTTTACCAT 1500
TAACAAACAG CATAAGACAA ACGGGCAAAC GTCATAAGAC ATCTGTTTAA TATCATAATT 1560
CAGAAAGCTT TTTCTATGCT GTTTAGAGAA GGTGGGGTCT TGAATTTAAA AAGTGGTTAA 1620
GTCTCCTCTT CTAAACTGGT GACTGCTAAA CTGGCTGGCT TCCTCCTAAT CTCCAGCCCC 1680
TTTTCTGGTA ACTGCCCCGA GGTACCCACG TTTCTGCAAC CTGCTTCACA CTGCAGACCC 1740
TGGAGGTGCG TGTGGACCTG GGCTGACCTC AGCAGTCACC GCCACCAGTC AGGGCCACTG 1800
GGAGGAGGGG GCAGTCCTGC TATACACCCT GCCCTCTCGA ACCGCAAGTG CAGAGAGGCC 1860
GCAGGTCTGG GGGCCCTCCA TATTCCATAC ATAAACTAGT CCAATACAGT GGCTCATGTC 1920
TGTAATAGCA GCACTTTGTG AGGCAAAGGC AGGAGGATGG CTTGAGTTCA AGACCAGCCT 1980
GGGCAACATA GCAAGACAAC CTCTCTGCAA AAAAATGAAA AACTAGCCTG CTTGGGGTAG 2040
TGCACACCTG TGGTCCCAGC TACTCAGGAG GCTGAGACAG GAGGATCACC TGAGCCCAGG 2100
AGGTCGTGCT GAGCCATGGT TGCGCCACTG CACTCCAGTC TGACAGAGCA AGACCCTGTC 2160
TCTAAAAATA AATAAATAAT ATACATAAGC TATTTGTTCA TTGCAGTAGA GTCGCTATCT 2220
TAACCTGAAA TTTTTCCGTA ATATTTCTTT CCTGGTAGGG CAATAGCTTG AAAATGTGTC 2280
CTTCTCTCAA CTCTTTATTC TCGAATGATC ACCCTTAAAA 2320