EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS002-03039 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr14:55568840-55571130 
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
TGGATAAAGG ATTGTAGGAA TTCCTTCCAT TGTTCTTGTA ATTTTTCTGC AACATTGAAA 60
TTATATCAGA TTAAAAGGCC CTCCTCCAAC AAAGCAAACA AACCTATGAG TGTGGCCAGG 120
AATCAGGCAA CACTTTGGCA AGAGCAACCG GGAGGCCTGT GCTTCCTGCT GGGGCCAGAG 180
CCAGCCCCAA ATACGTCCAC CCAGGGCCTG CAGGAGGGCA TGAATAGCGA CCCTGTAGGG 240
TAGGCCTGGT TGGCAAGAGC ACGTATTATG CAAATTCTGT CAACAACTAG ACCACAAGCT 300
GGGTTGCAGT TCCTGGCAGA ACTCATTATG TCCTTAGAGC AGAGAGGCCT TACAGCTGTT 360
TCGTGTTAGA TGATTCACAG ACAACGTGCA GCAAACCGAA GAATCATTGG TGAATGTGTG 420
AATTGCATTT GCATTTCATC TCTTTTCATA AAAATTATTG TTTAAGTCTG CTTTTGTTAC 480
AGCTCACTAA TAAATGGAGT GTATTTGCAT TTTTGCAAGG AGGCCTGAAT TTTTAACACC 540
TAATCATCTT TACCAAAGAG CAAGAATCGG CTAAAGTTTT CCCATTTAGT AAGAGTAGTA 600
ATTAAGACAT ACACCTTCCC TAAGCAATTC CTTTTCAAAA AGGAGCACAC ATTTAAAGAT 660
AACTCATTAA TATCTCTTCT GAGGCTGTTT ATCCAGTTTT GTCATGGCTC TAGAGCACAG 720
GAATCTTTTT TTCTCCTCCA TCTCTTTTTT AGCCAGTCTC TGAGAATCTC TGAGTTGCTA 780
AGTATTATTT ATTTCTTCCA TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT 840
TCGTTTTTTG AGCAACTTGA ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC 900
TTCTTCACAC AACCCCTAGT TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA 960
GGTGGCCAGC TCTAAAACCA ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC 1020
CTCCGGGTTA TGCCTGGTTA ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG 1080
AGGAGTGAAA CAGACAAAGA TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA 1140
AACTCCCATC CCGGATCACG CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA 1200
CATGACTGAA GAGGCCCTGC CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG 1260
AGTCATCTGG GTGTGGAGGC TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC 1320
AGGCAGAGAA CATCTAGACT GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG 1380
CATTCCCTAC TCTGTGAGCG TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA 1440
AGGCCAGTCA GTGCTATACA GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA 1500
AAGTTATGGG GCAGTGACTT CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC 1560
CTAGCTGAAC AGAATTTATC AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC 1620
AAAGAGAAAT GCTTTGGAAT TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA 1680
CTGGAAGACG AAAATCCAGG TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG 1740
CACCTGAAGA CTCACAGACA AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC 1800
CATTTCTTTG AGGTCATGAT CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC 1860
CCTATGAGTA AATGCTTCAG ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA 1920
CTAACACCCT GGTGTGACAG CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA 1980
CATCACCAAC CTGACATTTA ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG 2040
AATGGGGAAA TAGATGCTTT CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC TACTTCCTGA 2100
GCTGGGCTGG GAGCAACAGA AAAGAGAAGG AAGGAGAAAC CCAGCAAGGC AAGAGCAGCT 2160
CCTTCCCTTC TTTGACACAT TTATGTTCTG CTCCTATAGT GGTGGAAGCA GGAAGTAGGG 2220
TGACTGGCCT GCTCCACTCA CATTCTGATC ATTTTCTCTA CAAGGCAAGG ATGGCTAGCA 2280
CCTCCAGTTG 2290