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

TagContent
EnhancerAtlas ID
HS100-00098 
Organism
Homo sapiens 
Tissue/cell
HT1080 
Coordinate
chr14:55569400-55571220 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr14:55570002-55570012GGGGCGGGGC-6.02
LBX2MA0699.1chr14:55569718-55569728GCCAATTAGC+6.02
TBXTMA0009.2chr14:55570761-55570777TAACACCCTGGTGTGA-6.2
TBXTMA0009.2chr14:55570761-55570777TAACACCCTGGTGTGA+6.41
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00244chr14:55563236-55576350Adipose_Nuclei
SE_00820chr14:55569710-55569933Adipose_Tissue
SE_00820chr14:55570220-55570627Adipose_Tissue
SE_02600chr14:55568405-55571441Astrocytes
SE_09388chr14:55568067-55576360CD14
SE_23110chr14:55569439-55572086Colon_Crypt_1
SE_23790chr14:55569549-55571705Colon_Crypt_2
SE_24786chr14:55568610-55571711Colon_Crypt_3
SE_26013chr14:55568329-55572045Duodenum_Smooth_Muscle
SE_26711chr14:55567642-55572310Esophagus
SE_27630chr14:55568256-55572821Fetal_Intestine
SE_28543chr14:55567548-55572997Fetal_Intestine_Large
SE_31668chr14:55569464-55571780Gastric
SE_33558chr14:55567245-55572042H2171
SE_34039chr14:55568374-55571928HCC1954
SE_34802chr14:55567662-55571944HeLa
SE_36310chr14:55568260-55572008HMEC
SE_37768chr14:55568071-55572110HSMMtube
SE_41170chr14:55568268-55571740Left_Ventricle
SE_42472chr14:55567635-55571940Lung
SE_44570chr14:55568270-55571944NHDF-Ad
SE_45117chr14:55568080-55571960NHLF
SE_46036chr14:55568077-55571810Osteoblasts
SE_46880chr14:55569583-55571299Ovary
SE_49010chr14:55569384-55571714Right_Atrium
SE_50181chr14:55568296-55571959Sigmoid_Colon
SE_52430chr14:55568292-55571855Small_Intestine
SE_56717chr14:55568352-55571704u87
SE_57551chr14:55569509-55570126VACO_503
SE_57551chr14:55570182-55571719VACO_503
SE_64542chr14:55568330-55571772NHEK
SE_66903chr14:55567245-55572042H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr145557084555571098
chr145556973355570176
Number: 1             
IDChromosomeStartEnd
GH14I055097chr145556377555576469
Enhancer Sequence
CAAGAATCGG CTAAAGTTTT CCCATTTAGT AAGAGTAGTA ATTAAGACAT ACACCTTCCC 60
TAAGCAATTC CTTTTCAAAA AGGAGCACAC ATTTAAAGAT AACTCATTAA TATCTCTTCT 120
GAGGCTGTTT ATCCAGTTTT GTCATGGCTC TAGAGCACAG GAATCTTTTT TTCTCCTCCA 180
TCTCTTTTTT AGCCAGTCTC TGAGAATCTC TGAGTTGCTA AGTATTATTT ATTTCTTCCA 240
TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT TCGTTTTTTG AGCAACTTGA 300
ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC TTCTTCACAC AACCCCTAGT 360
TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA GGTGGCCAGC TCTAAAACCA 420
ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC CTCCGGGTTA TGCCTGGTTA 480
ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG AGGAGTGAAA CAGACAAAGA 540
TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA AACTCCCATC CCGGATCACG 600
CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA CATGACTGAA GAGGCCCTGC 660
CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG AGTCATCTGG GTGTGGAGGC 720
TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC AGGCAGAGAA CATCTAGACT 780
GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG CATTCCCTAC TCTGTGAGCG 840
TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA AGGCCAGTCA GTGCTATACA 900
GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA AAGTTATGGG GCAGTGACTT 960
CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC CTAGCTGAAC AGAATTTATC 1020
AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC AAAGAGAAAT GCTTTGGAAT 1080
TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA CTGGAAGACG AAAATCCAGG 1140
TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG CACCTGAAGA CTCACAGACA 1200
AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC CATTTCTTTG AGGTCATGAT 1260
CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC CCTATGAGTA AATGCTTCAG 1320
ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA CTAACACCCT GGTGTGACAG 1380
CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA CATCACCAAC CTGACATTTA 1440
ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG AATGGGGAAA TAGATGCTTT 1500
CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC TACTTCCTGA GCTGGGCTGG GAGCAACAGA 1560
AAAGAGAAGG AAGGAGAAAC CCAGCAAGGC AAGAGCAGCT CCTTCCCTTC TTTGACACAT 1620
TTATGTTCTG CTCCTATAGT GGTGGAAGCA GGAAGTAGGG TGACTGGCCT GCTCCACTCA 1680
CATTCTGATC ATTTTCTCTA CAAGGCAAGG ATGGCTAGCA CCTCCAGTTG TGTGGAATGC 1740
TTCTATCAGG GGCCTGTGTA CGGTATCATT GACATCTGGA ATGTCTCATT CAAGCAATGA 1800
GGGCCACGTG TGGTTGTGGA 1820