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

TagContent
EnhancerAtlas ID
HS092-37574 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr8:134497870-134499710 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr8:134498657-134498668CTGAGTCACCC-6.02
JUNBMA0490.1chr8:134498657-134498668CTGAGTCACCC-6.02
TBX20MA0689.1chr8:134498427-134498438CTTCACACCTA-6.62
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00507chr8:134497657-134498729Adipose_Nuclei
SE_00897chr8:134497803-134499300Adrenal_Gland
SE_04631chr8:134496712-134499381Brain_Anterior_Caudate
SE_08340chr8:134495384-134499766Brain_Inferior_Temporal_Lobe
SE_11515chr8:134491983-134499665CD20
SE_11962chr8:134497867-134498590CD3
SE_13062chr8:134497072-134498158CD34_Primary_RO01480
SE_13356chr8:134497349-134499198CD34_Primary_RO01536
SE_14091chr8:134497849-134499358CD34_Primary_RO01549
SE_14551chr8:134497673-134499097CD4_Memory_Primary_7pool
SE_17457chr8:134495478-134499314CD4p_CD25-_CD45RAp_Naive
SE_18016chr8:134497358-134499257CD4p_CD25-_CD45ROp_Memory
SE_18444chr8:134495757-134502590CD4p_CD25-_Il17-_PMAstim_Th
SE_19656chr8:134497535-134498810CD4p_CD25-_Il17p_PMAstim_Th17
SE_20094chr8:134497368-134499342CD56
SE_21569chr8:134497980-134499286CD8_Naive_7pool
SE_21937chr8:134497374-134499069CD8_Naive_8pool
SE_22340chr8:134496279-134499359CD8_primiary
SE_31509chr8:134498219-134499267Gastric
SE_40624chr8:134496637-134500070Left_Ventricle
SE_42148chr8:134496520-134499543Lung
SE_47079chr8:134496991-134499236Ovary
SE_48114chr8:134497225-134499441Psoas_Muscle
SE_48574chr8:134496813-134499355Right_Atrium
SE_50484chr8:134497913-134499350Sigmoid_Colon
SE_52693chr8:134497326-134499370Small_Intestine
SE_53366chr8:134497637-134499357Spleen
SE_62446chr8:134497139-134544764Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8134498200134499191
Number: 2             
IDChromosomeStartEnd
GH08I133484chr8134496558134499368
GH08I133487chr8134499601134499973
Enhancer Sequence
AAAGAAAACC AGATGCCCAA GTCCCAAGAC CCGCTTGACT CCTTAGAAAA AACCTGCTGT 60
ATTCTACAGG GTGGCTACCC CGGAGTAGGT GTTCTTCCCA TTCCCAGGGG CAGGATCTTA 120
GGAGGTGTCA TGGGCTGCAA CTGAAAAGAG AGGGTGGAGC TTTGGGGGGG ATAGAAGGTC 180
GGGAGTTGGT TTAGCTGCTG CCACAAGGGG TGGGGGGCTG TTTGCGGTGA CCCCCAGGAA 240
GTTACATGGG CTGCTGAGCC TCAAGTTCCT CATCCATAAA GCGGGGGTTA AAAACCATCC 300
CTACTTGAGG TGACTGCACA GAGCAGTAAT GTGTCAACAC TGAGGACACC TACCATCACC 360
TTTGTCTTTT CTATACTGTG TTCTAAGCAC AATACCGGTG CACATTGGCT GGGCCCACAA 420
CAAGCTCCCG ATGAAGGTAC TGGGTATCAT CTCCAGCTTT CAGAGCTGGG ACAGAGGCCC 480
ACAGTGGTCA AGCCACCTAC CCAAGGCCCT CGGCCGGTAG GTGTAAAGTC AGGATTACGG 540
CCAATGCAGA ATCCCAACTT CACACCTACT GGTGTGAAGT GGATGGTGCC AGGCTGAGGT 600
CGGCCCCTGC CCTGGGCCTC CTTGCTGTCT GAGCTGTGGA AGAGGAACCA GCCTATCCCC 660
ACTCCATGGT GGCACTGTGA GCACTGAGTG GGCTTTGTGT GTGGCGCAGC TCAGGGCCTG 720
GCAGGGGCGA GTGTGAGCCC TCCCTTCCCT TGTTTTGTTT TCTCCTTCCA GCTGGGCTCC 780
ACCCGCTCTG AGTCACCCCT GAAGCTGACA GCTGTGCTCT CATGGCCGAG CCAGGCCTGG 840
ACCCACTCAA CGCCGCTCTC CTCCCCTGGG TCAGGAAGGA TCAGCCGTGA GGGGAGCCAG 900
ACCCGTTTCC CTCCAGAAAA CATCATCCAA GAGAAACAGG GCCACAGTGA GGTGAGGCCT 960
GAGAGGAGGT CCTGGCCACT GCAAGGTAAA CAGGTGATGA CAAGCTCCCT GTCAATGGCA 1020
GGACTGGGGT GGACATTTCT CTCCTTATGT CGATTAAAAA AATCAGTCTC GAATGAAGCC 1080
AGCCAGCCAG CAACTGTGCT GCCCTGAGGC TCCCTGCGCC TCCCAGGAGA GGAGAGAACA 1140
CCCACCCCCA ACCCCAGGGA CAGCAGCCAC GGAGCACAGC GTGACTTGGG CCACTTCAGA 1200
AGCCGAGGCC AGTCAGCTCC TCATCTGTAA AATGCAACAA TGATCCCAGC CCCTGCTCAC 1260
CTAGACTTGG CTAATTGAAC AAATTAATGA CTATTGGTTA GTCCTGAGAG TCACTTTCTT 1320
ACTTCTTTTT TATTGAGACG GAGTCTCGCT CTGTTGCCCA GGCTGGAGTG CAGTGGTGTC 1380
ATCTTGGCTC ACCATAACTT CTGCCTCCCG GATTCAAGCG ATTCTCCTGC CTCAGCCTCT 1440
CGAGTAGCTG GGACTACAGA TGTGCACCAT GCCTGGTTCA TTTTTGTATT TTTAGTAGGG 1500
ACGGGGTTTT ACTATGTTGG CCAGGCTGGT CTCGAACTCC TGACCTCGTG ATCTGCCCAC 1560
CTTGGCCTCC CAAAGTGCTG GGATTACAGG CATGAGCTAC CACACCGTAC AATCATGTTA 1620
CTAATAATCT TGAATATTTA ACACATATTG GAAACAATAC TATTGGTATA TATATATATA 1680
TATAGTGCTT AGAACAATTC CTGACCATCA CAAAAGAATA TTTAACATTA ACATTAACAT 1740
TAGGAAAATG TCACCTACCC AGGATCATCA TTCCTCTGAG AAATTCAGAA CTGCATATGT 1800
GTGTGTGTGG ATAATGGCTA GTGGGGTTGA AAATGAAGAA 1840