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

TagContent
EnhancerAtlas ID
HS052-34339 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr7:2773890-2775780 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs798526chr72775542hg19
rs33932857chr72775718hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr7:2774786-2774807TCTCCTGCCTCCTCCTGCTCT-6.27
ZNF263MA0528.1chr7:2774780-2774801CCTCTCTCTCCTGCCTCCTCC-7.29
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_08508chr7:2774377-2775864Brain_Inferior_Temporal_Lobe
SE_13053chr7:2772498-2776851CD34_Primary_RO01480
SE_13522chr7:2770820-2777015CD34_Primary_RO01536
SE_14094chr7:2767596-2779169CD34_Primary_RO01549
SE_65933chr7:2772654-2777111Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr727740332775600
Number: 1             
IDChromosomeStartEnd
GH07I002727chr727673502775713
Enhancer Sequence
ACAGAGCAGC CCGCATATGA ACAGGCACGC AATGAGTCCC TTCAAAGGTA GCGTATTAAA 60
AACCAATTAT ACCACTTTCT ATAAGATTCC ACTTTGAACC CTGCTCTAAA GACAGACACC 120
AGCAGGCGGG GTCAAGGCTT CCAGGCTGCC CTGACATCAG GGCTTGTGGG AAGAGCAGTC 180
ACTTTCTGTG TTCTCATGGA AATGTACAGG GGCAAGGTCA TACACATGTG GCGAGCTGAC 240
GCAGGAGAAT TTTAAGGAGA GAAGGCCATC AGAATGGACT ACGTGATGGC GCTGAAGCTC 300
GTGGCGTTGT AAGGGATGGA GAAAGGCGGC CAGCACCTGC TCAGTCTATC TCTTCCTCCT 360
CTGTCCCAGA CAGACTGAGG GGAGAAAGCA GAGAGGAAGC TCCTTCAGGG AGGAGCCCAC 420
CTTCCTACTT TAGAACGAAG GCCTCTGGAT GTTTTCAAAG TGAGTGTTTT GTTTGAGGGG 480
ACAGAAACAC ACGTCTCCCC ATCCCAGCAC TGCCTGTGTT GAGCGAGCAC ACATCCTCCT 540
CCTCTGTGGC AGGACGGGGC GAGCACGTGC ACCTCGTGAC CACCGGCTCT CTAGAGCCCC 600
AGGCAGAGGC CCAGCTCTGC AGTAGGGAAG GCATCGGGAG TGCCAGGGTG AACGTACCCC 660
AAGGGCCCGG CACGACTGAC CTCTCGTGCC TGCTCTCTCC CTTCCTCGCC AAGCCCCCGT 720
GATGTGGGAA GCCAGCGTGA GGCCGGTGGG GCAGCCGCCT TCCCGTGGCT GTGCCAAGTC 780
CCCCCGGTCC TCTGCACATC ATGCCTCCTT CCACACCCTG ACAGGAAGCA GCTGGGAGAA 840
GCCGTTGGGT GCACTCACTC CCTGATTTAC GACAAGTTCC TTCCTCAGCG CCTCTCTCTC 900
CTGCCTCCTC CTGCTCTCCT GCCCTCCCCT GGGCCTCGGG AGGTGCCACG CAAGCCCAAG 960
AAGCATCAGC ATACTGTCCC TCCCTCTCCT GTGGCCACGG GCTCCCCCAG GGAGCTGAGA 1020
GTAGCAGCAG CTCACAGCCC AAGCCACCCT TGCCCGTTTC TAGGCAGGTG GTGGCACCAG 1080
GCACGAAGGA AGCAGAGGCA GTTCTCCTGC AGGGTTCTAG CTGGGTCAGG CATGGAGAGT 1140
CACAGTGGCA CAGATGCCCC AGCCAGTGCT CTTATCACCA CAGGACACAA AGCCCTGGAC 1200
ACACGTGCTC CGCCCAGATA GTACGGACGC AAGGGGAAAA GCACCACAGA GGGCACAATC 1260
AGGACAAGCT CGATGGGAAG CAGAAAACAG GAGGGACGTT TCCCTCGGTG TGAGTCTAAA 1320
CACCCCTCGA GTCTGCAATC AGTCCCCCAG CTGCACTTCA CAACACAGCA AACACTCACT 1380
GCTGCTTTCT CCACGATGAC TGAATGAGGA TGGCTCATTT AACTCATCAC AGCATTTGTA 1440
TCACTACTTG GAATGCAGGA AAACTTATCT GTGACTCTCG GTCATCTTGC ATGAGTGGCG 1500
GAGGAGAGGA GTCAAATCTA GTTTCATGTC AGGGCGGCCT CATCTCGAGA AACAGCCCAG 1560
GGGGTCCGTG GGAAAGCTGC CACTGAACTG TAAGGTGCCA GGGACTGTGC CACAAGCTCT 1620
CTAATGGGGG CTGGAGGGGA GGGAAGAAGG GGACACAGAG CAACCCTGTG TGATCCAGAA 1680
CGCTGTCACT CACATCCGCA CTCTTGCTGT CCCTGAGGTT TGGTGCACTG CGGTTCACCA 1740
ACAGAGACTG GACAATGCAC CTGCTGATTG GGCACGCAGC CCACGGGACG ATCGTTTGCG 1800
ACGGACTCCT CAAGTCTTAC AGCAGCAGCT CATTAAAAGG GCCAGGTTTA CAATCCCATG 1860
CATTTTCAAC ACTAAGAGAA TTCAGTCATT 1890