EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS056-04360 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr14:55568360-55570980 
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
CAGCCTGGGC AACAGAGTGA GACTCCATCT CAAAAAAAAA GAAAAAAAAA AAGCACACTG 60
AAGTTTTCAA GTTACTTTTT ATTTTTTTTG AGACAGGTCT CGCTCTGTTG CCCAGGCTGG 120
AGTATAGTGG CACGATCATG GCTCACTCTG CAACGCAACC TCAACCTCCT GGGCCTAAGT 180
GATCCTCCCA CCTCAGCCTC CTGAATAGCT GGGACCGCAG GCACATGCCA CCACGTCCAG 240
CTAACTTTTT TATTTTGGGT GGAGACAGGG GTCTCCCTAT GTTGCCCAGG CTGGTCTCAA 300
ACTCATGACC TCAAGCAATC CTCCTGCCTT GGCCTCCCAA AGTGCTGCAA TTACAGCCAT 360
GAGCCACTGT GCTCAACCAA CAATTTACTC TTAAATGTTG CTATATATAC ATATATATAT 420
CACACATACA TATTTATGGA TAGAGAATGT TAAGACAAAA ATGGAAACCA TCAGTGACTC 480
TGGATAAAGG ATTGTAGGAA TTCCTTCCAT TGTTCTTGTA ATTTTTCTGC AACATTGAAA 540
TTATATCAGA TTAAAAGGCC CTCCTCCAAC AAAGCAAACA AACCTATGAG TGTGGCCAGG 600
AATCAGGCAA CACTTTGGCA AGAGCAACCG GGAGGCCTGT GCTTCCTGCT GGGGCCAGAG 660
CCAGCCCCAA ATACGTCCAC CCAGGGCCTG CAGGAGGGCA TGAATAGCGA CCCTGTAGGG 720
TAGGCCTGGT TGGCAAGAGC ACGTATTATG CAAATTCTGT CAACAACTAG ACCACAAGCT 780
GGGTTGCAGT TCCTGGCAGA ACTCATTATG TCCTTAGAGC AGAGAGGCCT TACAGCTGTT 840
TCGTGTTAGA TGATTCACAG ACAACGTGCA GCAAACCGAA GAATCATTGG TGAATGTGTG 900
AATTGCATTT GCATTTCATC TCTTTTCATA AAAATTATTG TTTAAGTCTG CTTTTGTTAC 960
AGCTCACTAA TAAATGGAGT GTATTTGCAT TTTTGCAAGG AGGCCTGAAT TTTTAACACC 1020
TAATCATCTT TACCAAAGAG CAAGAATCGG CTAAAGTTTT CCCATTTAGT AAGAGTAGTA 1080
ATTAAGACAT ACACCTTCCC TAAGCAATTC CTTTTCAAAA AGGAGCACAC ATTTAAAGAT 1140
AACTCATTAA TATCTCTTCT GAGGCTGTTT ATCCAGTTTT GTCATGGCTC TAGAGCACAG 1200
GAATCTTTTT TTCTCCTCCA TCTCTTTTTT AGCCAGTCTC TGAGAATCTC TGAGTTGCTA 1260
AGTATTATTT ATTTCTTCCA TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT 1320
TCGTTTTTTG AGCAACTTGA ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC 1380
TTCTTCACAC AACCCCTAGT TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA 1440
GGTGGCCAGC TCTAAAACCA ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC 1500
CTCCGGGTTA TGCCTGGTTA ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG 1560
AGGAGTGAAA CAGACAAAGA TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA 1620
AACTCCCATC CCGGATCACG CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA 1680
CATGACTGAA GAGGCCCTGC CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG 1740
AGTCATCTGG GTGTGGAGGC TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC 1800
AGGCAGAGAA CATCTAGACT GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG 1860
CATTCCCTAC TCTGTGAGCG TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA 1920
AGGCCAGTCA GTGCTATACA GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA 1980
AAGTTATGGG GCAGTGACTT CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC 2040
CTAGCTGAAC AGAATTTATC AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC 2100
AAAGAGAAAT GCTTTGGAAT TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA 2160
CTGGAAGACG AAAATCCAGG TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG 2220
CACCTGAAGA CTCACAGACA AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC 2280
CATTTCTTTG AGGTCATGAT CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC 2340
CCTATGAGTA AATGCTTCAG ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA 2400
CTAACACCCT GGTGTGACAG CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA 2460
CATCACCAAC CTGACATTTA ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG 2520
AATGGGGAAA TAGATGCTTT CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC TACTTCCTGA 2580
GCTGGGCTGG GAGCAACAGA AAAGAGAAGG AAGGAGAAAC 2620