EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS117-02199 
Organism
Homo sapiens 
Tissue/cell
LHCN-M2 
Coordinate
chr14:55569300-55571110 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr14:55570002-55570012GGGGCGGGGC-6.02
LBX2MA0699.1chr14:55569718-55569728GCCAATTAGC+6.02
TBXTMA0009.2chr14:55570761-55570777TAACACCCTGGTGTGA-6.2
TBXTMA0009.2chr14:55570761-55570777TAACACCCTGGTGTGA+6.41
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00244chr14:55563236-55576350Adipose_Nuclei
SE_00820chr14:55569710-55569933Adipose_Tissue
SE_00820chr14:55570220-55570627Adipose_Tissue
SE_02600chr14:55568405-55571441Astrocytes
SE_09388chr14:55568067-55576360CD14
SE_23110chr14:55569439-55572086Colon_Crypt_1
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_31668chr14:55569464-55571780Gastric
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_46880chr14:55569583-55571299Ovary
SE_49010chr14:55569384-55571714Right_Atrium
SE_50181chr14:55568296-55571959Sigmoid_Colon
SE_52430chr14:55568292-55571855Small_Intestine
SE_56717chr14:55568352-55571704u87
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
chr145557084555571098
chr145556973355570176
Number: 1             
IDChromosomeStartEnd
GH14I055097chr145556377555576469
Enhancer Sequence
TTTAAGTCTG CTTTTGTTAC AGCTCACTAA TAAATGGAGT GTATTTGCAT TTTTGCAAGG 60
AGGCCTGAAT TTTTAACACC TAATCATCTT TACCAAAGAG CAAGAATCGG CTAAAGTTTT 120
CCCATTTAGT AAGAGTAGTA ATTAAGACAT ACACCTTCCC TAAGCAATTC CTTTTCAAAA 180
AGGAGCACAC ATTTAAAGAT AACTCATTAA TATCTCTTCT GAGGCTGTTT ATCCAGTTTT 240
GTCATGGCTC TAGAGCACAG GAATCTTTTT TTCTCCTCCA TCTCTTTTTT AGCCAGTCTC 300
TGAGAATCTC TGAGTTGCTA AGTATTATTT ATTTCTTCCA TTTTACCCCC AGGAGCTTAG 360
CCATTTTTGA TTTTTTGGCT TCGTTTTTTG AGCAACTTGA ATGTCCCACA CATCAAAGGC 420
CAATTAGCTA AAAGACAGGC TTCTTCACAC AACCCCTAGT TGATATCAAC CTGTCTTTTT 480
CTCAAAGCAA CAGGAAGCCA GGTGGCCAGC TCTAAAACCA ATCCCACCAC ATAACGTTTT 540
TCCTAACCTC TGACTTACAC CTCCGGGTTA TGCCTGGTTA ACCTTCTCGT TTTCCTCCTG 600
GGGCCAAGAG TGAGCTGCTG AGGAGTGAAA CAGACAAAGA TTCACGTTCC TCTCCGGCCG 660
CCTATGGGGA GCAGTTTCCA AACTCCCATC CCGGATCACG CAGGGGCGGG GCAGTGCTAG 720
CCTGGGGAGC ACCTGGCCGA CATGACTGAA GAGGCCCTGC CCCAGAAAGG CCTCAAAAAC 780
ACTCGTTAAA GCTAGGGCTG AGTCATCTGG GTGTGGAGGC TGTCGGGTCA CATTCTTGAA 840
ACATAACAGG CAAACAGGAC AGGCAGAGAA CATCTAGACT GTGGATTCTG TAAAGCTTTT 900
TCAAGGCCAG TTCACAGAAG CATTCCCTAC TCTGTGAGCG TGAAATATAA AGGTGAATGC 960
AGCCCCAGTG CCAGCACATA AGGCCAGTCA GTGCTATACA GGGTCAGCTT AGCCCTGGGC 1020
TGACCCTTAA GATCAGGAAA AAGTTATGGG GCAGTGACTT CTCAGCAAGT CTTTTCCATG 1080
TTTCTGGTGT CTTCGAATTC CTAGCTGAAC AGAATTTATC AAAGCAGAAG GTAGCTGTTT 1140
ATACCCCAGT TTACCCAGGC AAAGAGAAAT GCTTTGGAAT TGAGATATTT TCAGGGCATG 1200
AGTGGTTTAG ATCTCTGAAA CTGGAAGACG AAAATCCAGG TTATTAGAGA TCAGCAGCAC 1260
CTGAGAGGCA GGCTTCCTGG CACCTGAAGA CTCACAGACA AGCCTTGGTA GCCTGGCTTG 1320
TTTTCCTTGC AGTTCAAAAC CATTTCTTTG AGGTCATGAT CTGAAAGGGG ACACTGGACC 1380
CTGAGACCTA AATTCTGGTC CCTATGAGTA AATGCTTCAG ACAGATCAAG TTGGGGAGCT 1440
TCCACTGAAA AACACTGAGA CTAACACCCT GGTGTGACAG CCACACCTGT CTCCAAAGTG 1500
TACACACCAC CCCACCAGGA CATCACCAAC CTGACATTTA ATTAGCAATG AGACACTTGT 1560
TTTCACTCCT GTGGTCAAAG AATGGGGAAA TAGATGCTTT CTGTCTCCTT GCCTTTGGTT 1620
ATTTTTCTCC TACTTCCTGA GCTGGGCTGG GAGCAACAGA AAAGAGAAGG AAGGAGAAAC 1680
CCAGCAAGGC AAGAGCAGCT CCTTCCCTTC TTTGACACAT TTATGTTCTG CTCCTATAGT 1740
GGTGGAAGCA GGAAGTAGGG TGACTGGCCT GCTCCACTCA CATTCTGATC ATTTTCTCTA 1800
CAAGGCAAGG 1810