EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-08068 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr14:55568500-55571230 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr14:55570002-55570012GGGGCGGGGC-6.02
LBX2MA0699.1chr14:55569718-55569728GCCAATTAGC+6.02
POU2F2MA0507.1chr14:55569263-55569276TGCATTTGCATTT+6.16
Pou2f3MA0627.1chr14:55569103-55569119TATTATGCAAATTCTG+6.11
TBXTMA0009.2chr14:55570761-55570777TAACACCCTGGTGTGA-6.2
TBXTMA0009.2chr14:55570761-55570777TAACACCCTGGTGTGA+6.41
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00244chr14:55563236-55576350Adipose_Nuclei
SE_00820chr14:55570220-55570627Adipose_Tissue
SE_02600chr14:55568405-55571441Astrocytes
SE_09388chr14:55568067-55576360CD14
SE_23110chr14:55568342-55569436Colon_Crypt_1
SE_23110chr14:55569439-55572086Colon_Crypt_1
SE_23790chr14:55568791-55569345Colon_Crypt_2
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_31668chr14:55568309-55569461Gastric
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_46880chr14:55568888-55569293Ovary
SE_46880chr14:55569583-55571299Ovary
SE_49010chr14:55568296-55569297Right_Atrium
SE_49010chr14:55569384-55571714Right_Atrium
SE_50181chr14:55568296-55571959Sigmoid_Colon
SE_52430chr14:55568292-55571855Small_Intestine
SE_56717chr14:55568352-55571704u87
SE_57551chr14:55568765-55569318VACO_503
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: 3             
ChromosomeStartEnd
chr145556903355569319
chr145557084555571098
chr145556973355570176
Number: 1             
IDChromosomeStartEnd
GH14I055097chr145556377555576469
Enhancer Sequence
GCTCACTCTG CAACGCAACC TCAACCTCCT GGGCCTAAGT GATCCTCCCA CCTCAGCCTC 60
CTGAATAGCT GGGACCGCAG GCACATGCCA CCACGTCCAG CTAACTTTTT TATTTTGGGT 120
GGAGACAGGG GTCTCCCTAT GTTGCCCAGG CTGGTCTCAA ACTCATGACC TCAAGCAATC 180
CTCCTGCCTT GGCCTCCCAA AGTGCTGCAA TTACAGCCAT GAGCCACTGT GCTCAACCAA 240
CAATTTACTC TTAAATGTTG CTATATATAC ATATATATAT CACACATACA TATTTATGGA 300
TAGAGAATGT TAAGACAAAA ATGGAAACCA TCAGTGACTC TGGATAAAGG ATTGTAGGAA 360
TTCCTTCCAT TGTTCTTGTA ATTTTTCTGC AACATTGAAA TTATATCAGA TTAAAAGGCC 420
CTCCTCCAAC AAAGCAAACA AACCTATGAG TGTGGCCAGG AATCAGGCAA CACTTTGGCA 480
AGAGCAACCG GGAGGCCTGT GCTTCCTGCT GGGGCCAGAG CCAGCCCCAA ATACGTCCAC 540
CCAGGGCCTG CAGGAGGGCA TGAATAGCGA CCCTGTAGGG TAGGCCTGGT TGGCAAGAGC 600
ACGTATTATG CAAATTCTGT CAACAACTAG ACCACAAGCT GGGTTGCAGT TCCTGGCAGA 660
ACTCATTATG TCCTTAGAGC AGAGAGGCCT TACAGCTGTT TCGTGTTAGA TGATTCACAG 720
ACAACGTGCA GCAAACCGAA GAATCATTGG TGAATGTGTG AATTGCATTT GCATTTCATC 780
TCTTTTCATA AAAATTATTG TTTAAGTCTG CTTTTGTTAC AGCTCACTAA TAAATGGAGT 840
GTATTTGCAT TTTTGCAAGG AGGCCTGAAT TTTTAACACC TAATCATCTT TACCAAAGAG 900
CAAGAATCGG CTAAAGTTTT CCCATTTAGT AAGAGTAGTA ATTAAGACAT ACACCTTCCC 960
TAAGCAATTC CTTTTCAAAA AGGAGCACAC ATTTAAAGAT AACTCATTAA TATCTCTTCT 1020
GAGGCTGTTT ATCCAGTTTT GTCATGGCTC TAGAGCACAG GAATCTTTTT TTCTCCTCCA 1080
TCTCTTTTTT AGCCAGTCTC TGAGAATCTC TGAGTTGCTA AGTATTATTT ATTTCTTCCA 1140
TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT TCGTTTTTTG AGCAACTTGA 1200
ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC TTCTTCACAC AACCCCTAGT 1260
TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA GGTGGCCAGC TCTAAAACCA 1320
ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC CTCCGGGTTA TGCCTGGTTA 1380
ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG AGGAGTGAAA CAGACAAAGA 1440
TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA AACTCCCATC CCGGATCACG 1500
CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA CATGACTGAA GAGGCCCTGC 1560
CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG AGTCATCTGG GTGTGGAGGC 1620
TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC AGGCAGAGAA CATCTAGACT 1680
GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG CATTCCCTAC TCTGTGAGCG 1740
TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA AGGCCAGTCA GTGCTATACA 1800
GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA AAGTTATGGG GCAGTGACTT 1860
CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC CTAGCTGAAC AGAATTTATC 1920
AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC AAAGAGAAAT GCTTTGGAAT 1980
TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA CTGGAAGACG AAAATCCAGG 2040
TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG CACCTGAAGA CTCACAGACA 2100
AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC CATTTCTTTG AGGTCATGAT 2160
CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC CCTATGAGTA AATGCTTCAG 2220
ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA CTAACACCCT GGTGTGACAG 2280
CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA CATCACCAAC CTGACATTTA 2340
ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG AATGGGGAAA TAGATGCTTT 2400
CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC TACTTCCTGA GCTGGGCTGG GAGCAACAGA 2460
AAAGAGAAGG AAGGAGAAAC CCAGCAAGGC AAGAGCAGCT CCTTCCCTTC TTTGACACAT 2520
TTATGTTCTG CTCCTATAGT GGTGGAAGCA GGAAGTAGGG TGACTGGCCT GCTCCACTCA 2580
CATTCTGATC ATTTTCTCTA CAAGGCAAGG ATGGCTAGCA CCTCCAGTTG TGTGGAATGC 2640
TTCTATCAGG GGCCTGTGTA CGGTATCATT GACATCTGGA ATGTCTCATT CAAGCAATGA 2700
GGGCCACGTG TGGTTGTGGA TGGTGAGATA 2730