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

TagContent
EnhancerAtlas ID
HS184-13642 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr17:43488480-43490230 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs62064641chr1743488792hg19
rs111443054chr1743489162hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR3C1MA0113.3chr17:43489916-43489933GGGGACATGGTGTCCTT+6.07
NR3C1MA0113.3chr17:43489916-43489933GGGGACATGGTGTCCTT-6.1
NR3C2MA0727.1chr17:43489916-43489933GGGGACATGGTGTCCTT+6.08
NR3C2MA0727.1chr17:43489916-43489933GGGGACATGGTGTCCTT-6
ZNF263MA0528.1chr17:43489296-43489317GGAGGAGCTGGGTGGAGAGGG+6.03
ZNF263MA0528.1chr17:43488635-43488656CCATCTTGTCTTCCCTCCTCC-6.14
ZNF263MA0528.1chr17:43489306-43489327GGTGGAGAGGGGAGAGAAGAG+6.19
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_23758chr17:43485536-43490348Colon_Crypt_2
SE_27799chr17:43481721-43494066Fetal_Intestine
SE_28693chr17:43481449-43494249Fetal_Intestine_Large
SE_42602chr17:43485387-43490334Lung
SE_52651chr17:43485072-43491303Small_Intestine
Enhancer Sequence
GGGCCAGGCA CCAGCTTCTT CCAGGAGGAA GGTTAAATCT TCTTCCTGGC CTCTCTTCCC 60
TTCACCCCCT CGTGTGGGGA TGACAGACCC CAGCCACGCA CAGTGGACAC ATGCCCTGAG 120
TAAGAAGTTA CAGCCCCTCC TCTGAGCCCA TGGGTCCATC TTGTCTTCCC TCCTCCCTTA 180
GAAGTGCTTC CTCCCCAGGC TTAAGGGCCA GGCAGCACTA AGCCCACCAG CCCACCCCTG 240
CTGAAGTCCA CCTCCTTTCC TGGTCAGGCT CTGACCCCCA CCCTTCCACT CTAGGCCCAT 300
TCTTCCTCCT CTGGCCCCCA CCCTGGATCT CTTTTTCTCC CCTGCCATGT CTCTCAGCCC 360
CTCTTCTCCT GTACCCACTG TGGGCTGGGG ACAAGGACCC CAAGCAGAGC CAGGCACAGT 420
GTGAATGTGG GGCACGAGAC ACTTGTAGAG ATCACACTAG GAGCAAGACT GGGCCCCATG 480
CCCTGCTCTG CCCACAAAAG CTCTCATACC AGTGTCCCAT CCCCTGTACC CGACTCAGAA 540
GCCCAGACCC CAGGGGTAGA CTAATCCCCT CCTCGCTATC AGGGTGGAGG ACAGCAGGAA 600
TCACAGAAGG CTGGAGGCCT CATGCTTATC ACACACCTGA CCCATCTCTC TGTCCCCACC 660
CTGAGGCCAG GGATGAGGAC TCACACACAC ACACACACAC ACACACTACA CACGTGTGCG 720
TGCATATGAC AGGTCACCAA GGGTTATGCA ACCAGGCCTC AGAGACAGGA ATAGCCTCTG 780
TAAATTCCAG AGAGGCCAGA AACTCTGAGC CACCAGGGAG GAGCTGGGTG GAGAGGGGAG 840
AGAAGAGGAC AGGTGTGGAA CTCAGGCCCT CAGCATTGCC CTGCAGGTAG CATGGGGGGC 900
AGGGACTCCC TATGGCAGAG CCAGGAGTGT CAGTGTCAGG GCTGGGACTG CAGAATGGGC 960
AGCCAGCAAC TCACCTGGCA TCTCACCTGC TTCTCTTCCC CAGTAGGAAG CTGGGCCCCC 1020
ATGATGGGGG TCTCCCAGGG GGCTCCAGCC CCAAACTATA GGGAGTGAAC AAACTCACAC 1080
AGTTCCTGCC TGCTCTTGGC CACAGAAGTT GGCTCTCAGG CCCTGTCTCG GATTCCCTCC 1140
CCCCAGTGAG AGGAGGTGAT GACCACAGTG GCTCCCCAGA GGGGTCCACC TCCCTCCACC 1200
ACACCCTCAT GCCTCTGAGA GGCACAAGGG GGAGGGTCAG GAGAGGTTCT AGAACAAACC 1260
AGCTGCACAA CACCCCTCCT TTCCCCACTC TGACCTCACT CTTCCCTCCC AAACCCTCAT 1320
AGGAAGTGCT GGGGCAGGAG CAGGTGCACT AGGAAGACCC AGTCCTCTGG GGCTAGAGGC 1380
AAAATGAACG CCTCCAAACC AGGACTTGGC CCAGGAACTG GCTCAGGGGC TGGCGAGGGG 1440
ACATGGTGTC CTTTGTTGAC TCAGTGAGTC TGCTCTGTGC CACCCAAGCC AGGTGGAGGG 1500
AGAGCCAGAA GGAATGGTGA TCTTTGCCTC AAGGAGCTCA GTCATGTCCA CACGACAGGT 1560
CCCTCCCCCA AACACATGTT CTCCAGGACA GAAACTGGGT CTCCCTTTAA CCATCCCGGC 1620
CTGGCCCAGA GCTACATGTC CAGGGGCAGG ATCGGAGGAG CTGGGGGTGA CCCCACAGGA 1680
TCCTGGGCCT CAGGCCTCAG TAGGCTTTGG GGAACTGTGC CTAGCTCAGC CCTCTGAGAT 1740
TCTGATGGAA 1750