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

TagContent
EnhancerAtlas ID
HS105-53293 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr22:37941020-37943860 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUNMA0488.1chr22:37941362-37941375ATGACCTCATCCT-6.23
JUND(var.2)MA0492.1chr22:37941361-37941376AATGACCTCATCCTT-6.35
KLF16MA0741.1chr22:37942155-37942166GCCCCGCCCCC+6.02
KLF5MA0599.1chr22:37942155-37942165GCCCCGCCCC+6.02
KLF5MA0599.1chr22:37942205-37942215GGGGCGGGGC-6.02
SP2MA0516.2chr22:37942151-37942168CTCAGCCCCGCCCCCAT+7.25
SP4MA0685.1chr22:37942152-37942169TCAGCCCCGCCCCCATC+6.32
Stat6MA0520.1chr22:37941455-37941470ACTTCTCTAGAAGTG-6.13
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00910chr22:37940961-37944411Adrenal_Gland
SE_01977chr22:37941111-37944503Aorta
SE_03448chr22:37941211-37943982Brain_Angular_Gyrus
SE_04244chr22:37940752-37944223Brain_Anterior_Caudate
SE_05121chr22:37940691-37944413Brain_Cingulate_Gyrus
SE_05970chr22:37940548-37949654Brain_Hippocampus_Middle
SE_06854chr22:37940943-37949244Brain_Hippocampus_Middle_150
SE_08232chr22:37940770-37944365Brain_Inferior_Temporal_Lobe
SE_26741chr22:37939854-37943980Esophagus
SE_27829chr22:37940816-37944045Fetal_Intestine
SE_28991chr22:37940998-37944015Fetal_Intestine_Large
SE_30047chr22:37940811-37944647Fetal_Muscle
SE_34331chr22:37940943-37943837HCT-116
SE_35499chr22:37940690-37943792HepG2
SE_36256chr22:37939917-37942804HMEC
SE_37242chr22:37940694-37950215HSMMtube
SE_41277chr22:37941066-37944006Left_Ventricle
SE_42365chr22:37940909-37944471Lung
SE_46750chr22:37941304-37943895Ovary
SE_47469chr22:37941043-37943865Pancreas
SE_48974chr22:37941283-37944006Right_Atrium
SE_54046chr22:37941162-37944428Spleen
SE_56081chr22:37940823-37944038u87
SE_57306chr22:37941377-37942191VACO_400
SE_64898chr22:37940053-37942175NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223794206437942352
chr223794133837941400
Number: 1             
IDChromosomeStartEnd
GH22I037543chr223793991737946307
Enhancer Sequence
CCAGGGGAGT TCATAACTCA CCCAAGGTTA CACAGCTGGA AATTTGGAAG AGCCAAGACT 60
CTCTTCCCCA CCACAGAACA GCCTGTGCGA GCCGCCCCAG CGCCTGGAGG CACCGACCCA 120
GAGCGGGTCT CACAAGGCTG AAAACCTGGG GTCTTCCCAG GGCAGTAGGG CGGCTTCATG 180
GAACTAGAGG CTGTAGTCCC AGTCCCAGTC CCCAGGCCCT TCCCCTCGCC AAGTCTGCAT 240
AGCCACATCA AATTGTGGTG GTTCCTTTAC CAGGCTCCCC TCTGCCTTCC TGCCTGGGGC 300
AAAAGAGGGC GCTCCAGAGC CACAGAAAGT CCACTGGGAC AAATGACCTC ATCCTTCCAC 360
CCCAGCCCTC CACTCCCTAA AACCTCCCCT CCTTCCCTCA CCTGTGCCTT TCTCCAACCC 420
TATCATGTCA CTAGCACTTC TCTAGAAGTG CCATGCCTTT GGCCAGGTTG TTTCCTGGGC 480
CAGGCACACT CTTTCACAAT TTTAGGCTTC TATATTGAGA GGGTGGCCTC CTTCCTCCAG 540
GAAGCCCTCC CTGGCTGCCT CCTCTGAGCT AGCTAGCTCC AATGTGCCCC CACGGCCTCT 600
GGGGGATGAC TGCCCCAAGC ATCAACCATG TTGTGCCCTA AGGGGCTGGG GTCCGGGAGG 660
GGAGACGAGG ACAGGGGTCA CCTACCTCCT TTTGGGTTAG GTGAGGGAGC GTGTGGGGGA 720
TGGGGCAGGC CTCCCTCTGC CCGGCCTCTT CTGGACCAGC GACCCTGACC CTCAGGCCCT 780
CGGTCAATAC CCATTGGGCA ACTACAGGAT CGATCGGCTG GGGCTGCCTG GAGGGGGAGG 840
TAGGCAGGGT TGTTTGCTTC CCCAGGGGCA CCTTTGGCCA GCCCCACCCC TCCGTGGAGG 900
TCTCCCCTGC CGGTCTCAGC CTCTTGACGT CCTCACCCCT CCTCTGGGAT TGTGCAGGCA 960
GCGGGGGGAA AAAGAGGGAG GCAGCAGCAG ATGGGGGCTG ACCCGGGAGC TGGCTCAACG 1020
CCCTGCCCTA GGGATGGAGA GACTGAGGCC GCCAGAGCCT GGTCAAGCCA GAGCTGAAGC 1080
CTCCGGCCCC AGCGGGACGG GAAGGAATCT GGTCTCCTCC TTCCTGGCTC CCTCAGCCCC 1140
GCCCCCATCA GAGCTGGGGA GGCCCCGGGA TGGGAGGAGA GGACTGGGGC GGGGCACCCA 1200
GACTTGGAGT GGGGCCTGGA GCCCGGGATG CTTCCTGCGG ACCTTCAACT CCCACATTCC 1260
AGGCTGTTCC CAAGACTCCT CGCTCCTCCT CCCTTCTCTA CCCATCCCGT GTTGCGGGCG 1320
GGGGCGCGGG TGTTAGTGGC CAGGGTCTGA GCTAGCTGCC TGGGGCCTGT GGGGGTACTC 1380
GGGGGCCCCT CCTAGGGAGG GATTAGATCT ACACTAGAGG GGCTGCCCTG GAGGCCTGTC 1440
CAAGCACCAC CCAAGGGTAC TTGTGATTGT CGTAAACAGG AAGCCCCCCT TTCCCCACCG 1500
CACCATGTAG ACAGGCCCTG TGTGTCCAGA CGCTGCGCTC TGGAGGCCGG GGGCTCTTGA 1560
CCTCCCCGGC TGCGTTTCCT GTTAGCTGAG CCAGAGGAGA AAGAAGGGGA CTGAAATGGG 1620
CTGGACAGGG GAGGTGCCTC AGGGAGTGAG AGCAGAAGGG GAAAGAGCCA AGGAGTGAAA 1680
GGCCAGAGCT GCCTGGCACA CAGTAGGTGG TCAATAGTCT GTGGCCTGAG GTTGGGTAAG 1740
AAGGGAGGGG CCCCTCTGAG GAGAGCCATA CAGTTGCCGG GAAGAGTGGA GGATTCACCC 1800
CACTGCCACC AAGGCCTGGC ACATAGTAGG TGCTCAGGAA ATATTTGAGA TCCATGTTTA 1860
GAGTAGGCCG GGAGGAGGCG TTCTTGGAAG AGAGCAGTGT TTCTGGAGAA GAAAATGAGG 1920
CCACCCCGGC CTTGCAGCCC GCTGCGGGCT CAGCATTCCC CCACCGTCCC TGTCTGGCCC 1980
CCGCCCCGCC CTGTGGCTGC CTGGGCCAGG CCACTGTCTC AAGGCCCTTT ATTTTTAAAA 2040
TCCCTGCGGT GTTCCTGCCC CAAGACTAAG GAGCAGTGCC AGCCAACAGC TCAGCCTGCG 2100
GCCTGGGCTC AGGGCCTAAA GGCGCCAGGG GTGGGGCATC TGGCCACCCC ACAGCTGCTG 2160
GCCCAGCCGG CCTGCCTGAG CAGGGTGAGG AGGCCCCTGG AATGCCCCCA CCCTGGGCCC 2220
GAGGCATTAG TCCTTAGTCC CTGGTGAAGG GACAGAGGCC CACAAGGGTG GCAAGCAGGC 2280
TTTGCATGTT GAATATAGTA GCTTGTTCCT CCCACATCTT CCAAACAAAT ACGGGCACAG 2340
CACCTACTGT GTGTAAGGAG GAGGCGCGAG CTGGACCTCG TGGGGTGACA AAGGGGTGAG 2400
ACATGCTTTC TCTTTTCCAG GGAGTCAGGG CCTGCAGAGG AAACAGGCAT CGCAGTTGTG 2460
GGCATTTCTT GAAAGAGCCA CGGACTGGAA TCTAAGAGGC CTCTGGGCCC CAGTCCTGGC 2520
TCCATCCCTT CCCAGCTGTG TGGACTTGGG CAAGGCATTT GGTCTCTCTA AGCTTCTCTA 2580
CAAAGGAAAA CAATCACAGC TACCATGGAA GGCTGCTGTC TGTCACTAGA CACAGCGATG 2640
AGCAACGCAG TCACCATCCC TGCCCTCACG GAGGTTAATG TCATGGGGGA AGGTGGTCCC 2700
CTGAACAAGG TCATGGCAGT CACCAGAGGC ACAGAGCAGC AGCACGGAAG GGAGGGTGCT 2760
GGGGGGCAGG GGTGGGAGAG AACTTAATTT ATGTGTTTTG GTTTTTTGAG ACAGAGTTTT 2820
CGCTTTTTCT GCCCAGGCTG 2840