EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS076-17548 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr14:55568350-55571070 
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
CACTGCACTC CAGCCTGGGC AACAGAGTGA GACTCCATCT CAAAAAAAAA GAAAAAAAAA 60
AAGCACACTG AAGTTTTCAA GTTACTTTTT ATTTTTTTTG AGACAGGTCT CGCTCTGTTG 120
CCCAGGCTGG AGTATAGTGG CACGATCATG GCTCACTCTG CAACGCAACC TCAACCTCCT 180
GGGCCTAAGT GATCCTCCCA CCTCAGCCTC CTGAATAGCT GGGACCGCAG GCACATGCCA 240
CCACGTCCAG CTAACTTTTT TATTTTGGGT GGAGACAGGG GTCTCCCTAT GTTGCCCAGG 300
CTGGTCTCAA ACTCATGACC TCAAGCAATC CTCCTGCCTT GGCCTCCCAA AGTGCTGCAA 360
TTACAGCCAT GAGCCACTGT GCTCAACCAA CAATTTACTC TTAAATGTTG CTATATATAC 420
ATATATATAT CACACATACA TATTTATGGA TAGAGAATGT TAAGACAAAA ATGGAAACCA 480
TCAGTGACTC TGGATAAAGG ATTGTAGGAA TTCCTTCCAT TGTTCTTGTA ATTTTTCTGC 540
AACATTGAAA TTATATCAGA TTAAAAGGCC CTCCTCCAAC AAAGCAAACA AACCTATGAG 600
TGTGGCCAGG AATCAGGCAA CACTTTGGCA AGAGCAACCG GGAGGCCTGT GCTTCCTGCT 660
GGGGCCAGAG CCAGCCCCAA ATACGTCCAC CCAGGGCCTG CAGGAGGGCA TGAATAGCGA 720
CCCTGTAGGG TAGGCCTGGT TGGCAAGAGC ACGTATTATG CAAATTCTGT CAACAACTAG 780
ACCACAAGCT GGGTTGCAGT TCCTGGCAGA ACTCATTATG TCCTTAGAGC AGAGAGGCCT 840
TACAGCTGTT TCGTGTTAGA TGATTCACAG ACAACGTGCA GCAAACCGAA GAATCATTGG 900
TGAATGTGTG AATTGCATTT GCATTTCATC TCTTTTCATA AAAATTATTG TTTAAGTCTG 960
CTTTTGTTAC AGCTCACTAA TAAATGGAGT GTATTTGCAT TTTTGCAAGG AGGCCTGAAT 1020
TTTTAACACC TAATCATCTT TACCAAAGAG CAAGAATCGG CTAAAGTTTT CCCATTTAGT 1080
AAGAGTAGTA ATTAAGACAT ACACCTTCCC TAAGCAATTC CTTTTCAAAA AGGAGCACAC 1140
ATTTAAAGAT AACTCATTAA TATCTCTTCT GAGGCTGTTT ATCCAGTTTT GTCATGGCTC 1200
TAGAGCACAG GAATCTTTTT TTCTCCTCCA TCTCTTTTTT AGCCAGTCTC TGAGAATCTC 1260
TGAGTTGCTA AGTATTATTT ATTTCTTCCA TTTTACCCCC AGGAGCTTAG CCATTTTTGA 1320
TTTTTTGGCT TCGTTTTTTG AGCAACTTGA ATGTCCCACA CATCAAAGGC CAATTAGCTA 1380
AAAGACAGGC TTCTTCACAC AACCCCTAGT TGATATCAAC CTGTCTTTTT CTCAAAGCAA 1440
CAGGAAGCCA GGTGGCCAGC TCTAAAACCA ATCCCACCAC ATAACGTTTT TCCTAACCTC 1500
TGACTTACAC CTCCGGGTTA TGCCTGGTTA ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG 1560
TGAGCTGCTG AGGAGTGAAA CAGACAAAGA TTCACGTTCC TCTCCGGCCG CCTATGGGGA 1620
GCAGTTTCCA AACTCCCATC CCGGATCACG CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC 1680
ACCTGGCCGA CATGACTGAA GAGGCCCTGC CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA 1740
GCTAGGGCTG AGTCATCTGG GTGTGGAGGC TGTCGGGTCA CATTCTTGAA ACATAACAGG 1800
CAAACAGGAC AGGCAGAGAA CATCTAGACT GTGGATTCTG TAAAGCTTTT TCAAGGCCAG 1860
TTCACAGAAG CATTCCCTAC TCTGTGAGCG TGAAATATAA AGGTGAATGC AGCCCCAGTG 1920
CCAGCACATA AGGCCAGTCA GTGCTATACA GGGTCAGCTT AGCCCTGGGC TGACCCTTAA 1980
GATCAGGAAA AAGTTATGGG GCAGTGACTT CTCAGCAAGT CTTTTCCATG TTTCTGGTGT 2040
CTTCGAATTC CTAGCTGAAC AGAATTTATC AAAGCAGAAG GTAGCTGTTT ATACCCCAGT 2100
TTACCCAGGC AAAGAGAAAT GCTTTGGAAT TGAGATATTT TCAGGGCATG AGTGGTTTAG 2160
ATCTCTGAAA CTGGAAGACG AAAATCCAGG TTATTAGAGA TCAGCAGCAC CTGAGAGGCA 2220
GGCTTCCTGG CACCTGAAGA CTCACAGACA AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC 2280
AGTTCAAAAC CATTTCTTTG AGGTCATGAT CTGAAAGGGG ACACTGGACC CTGAGACCTA 2340
AATTCTGGTC CCTATGAGTA AATGCTTCAG ACAGATCAAG TTGGGGAGCT TCCACTGAAA 2400
AACACTGAGA CTAACACCCT GGTGTGACAG CCACACCTGT CTCCAAAGTG TACACACCAC 2460
CCCACCAGGA CATCACCAAC CTGACATTTA ATTAGCAATG AGACACTTGT TTTCACTCCT 2520
GTGGTCAAAG AATGGGGAAA TAGATGCTTT CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC 2580
TACTTCCTGA GCTGGGCTGG GAGCAACAGA AAAGAGAAGG AAGGAGAAAC CCAGCAAGGC 2640
AAGAGCAGCT CCTTCCCTTC TTTGACACAT TTATGTTCTG CTCCTATAGT GGTGGAAGCA 2700
GGAAGTAGGG TGACTGGCCT 2720