EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS024-04542 
Organism
Homo sapiens 
Tissue/cell
Cerebellum 
Coordinate
chr14:55568480-55570910 
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: 2             
ChromosomeStartEnd
chr145556903355569319
chr145556973355570176
Number: 1             
IDChromosomeStartEnd
GH14I055097chr145556377555576469
Enhancer Sequence
AGTATAGTGG CACGATCATG GCTCACTCTG CAACGCAACC TCAACCTCCT GGGCCTAAGT 60
GATCCTCCCA CCTCAGCCTC CTGAATAGCT GGGACCGCAG GCACATGCCA CCACGTCCAG 120
CTAACTTTTT TATTTTGGGT GGAGACAGGG GTCTCCCTAT GTTGCCCAGG CTGGTCTCAA 180
ACTCATGACC TCAAGCAATC CTCCTGCCTT GGCCTCCCAA AGTGCTGCAA TTACAGCCAT 240
GAGCCACTGT GCTCAACCAA CAATTTACTC TTAAATGTTG CTATATATAC ATATATATAT 300
CACACATACA TATTTATGGA TAGAGAATGT TAAGACAAAA ATGGAAACCA TCAGTGACTC 360
TGGATAAAGG ATTGTAGGAA TTCCTTCCAT TGTTCTTGTA ATTTTTCTGC AACATTGAAA 420
TTATATCAGA TTAAAAGGCC CTCCTCCAAC AAAGCAAACA AACCTATGAG TGTGGCCAGG 480
AATCAGGCAA CACTTTGGCA AGAGCAACCG GGAGGCCTGT GCTTCCTGCT GGGGCCAGAG 540
CCAGCCCCAA ATACGTCCAC CCAGGGCCTG CAGGAGGGCA TGAATAGCGA CCCTGTAGGG 600
TAGGCCTGGT TGGCAAGAGC ACGTATTATG CAAATTCTGT CAACAACTAG ACCACAAGCT 660
GGGTTGCAGT TCCTGGCAGA ACTCATTATG TCCTTAGAGC AGAGAGGCCT TACAGCTGTT 720
TCGTGTTAGA TGATTCACAG ACAACGTGCA GCAAACCGAA GAATCATTGG TGAATGTGTG 780
AATTGCATTT GCATTTCATC TCTTTTCATA AAAATTATTG TTTAAGTCTG CTTTTGTTAC 840
AGCTCACTAA TAAATGGAGT GTATTTGCAT TTTTGCAAGG AGGCCTGAAT TTTTAACACC 900
TAATCATCTT TACCAAAGAG CAAGAATCGG CTAAAGTTTT CCCATTTAGT AAGAGTAGTA 960
ATTAAGACAT ACACCTTCCC TAAGCAATTC CTTTTCAAAA AGGAGCACAC ATTTAAAGAT 1020
AACTCATTAA TATCTCTTCT GAGGCTGTTT ATCCAGTTTT GTCATGGCTC TAGAGCACAG 1080
GAATCTTTTT TTCTCCTCCA TCTCTTTTTT AGCCAGTCTC TGAGAATCTC TGAGTTGCTA 1140
AGTATTATTT ATTTCTTCCA TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT 1200
TCGTTTTTTG AGCAACTTGA ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC 1260
TTCTTCACAC AACCCCTAGT TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA 1320
GGTGGCCAGC TCTAAAACCA ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC 1380
CTCCGGGTTA TGCCTGGTTA ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG 1440
AGGAGTGAAA CAGACAAAGA TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA 1500
AACTCCCATC CCGGATCACG CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA 1560
CATGACTGAA GAGGCCCTGC CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG 1620
AGTCATCTGG GTGTGGAGGC TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC 1680
AGGCAGAGAA CATCTAGACT GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG 1740
CATTCCCTAC TCTGTGAGCG TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA 1800
AGGCCAGTCA GTGCTATACA GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA 1860
AAGTTATGGG GCAGTGACTT CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC 1920
CTAGCTGAAC AGAATTTATC AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC 1980
AAAGAGAAAT GCTTTGGAAT TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA 2040
CTGGAAGACG AAAATCCAGG TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG 2100
CACCTGAAGA CTCACAGACA AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC 2160
CATTTCTTTG AGGTCATGAT CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC 2220
CCTATGAGTA AATGCTTCAG ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA 2280
CTAACACCCT GGTGTGACAG CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA 2340
CATCACCAAC CTGACATTTA ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG 2400
AATGGGGAAA TAGATGCTTT CTGTCTCCTT 2430