EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-15317 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr19:1856180-1857980 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10411759chr191857297hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:1856368-1856386TCATCCTTCCTCCCTGCC-6.08
KLF5MA0599.1chr19:1857129-1857139GCCCCGCCCC+6.02
SPIBMA0081.2chr19:1856870-1856882CACTTCCCCTTT-6.07
ZNF263MA0528.1chr19:1856360-1856381TTCTCATCTCATCCTTCCTCC-6.11
ZNF740MA0753.2chr19:1856952-1856965GTGGGGGGGGCGA-7.04
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_05653chr19:1854545-1857986Brain_Cingulate_Gyrus
SE_12493chr19:1856309-1856716CD34_adult
SE_12794chr19:1855785-1856406CD34_fetal
SE_12794chr19:1856478-1856737CD34_fetal
SE_15325chr19:1851179-1863643CD4_Memory_Primary_7pool
SE_17066chr19:1855162-1858408CD4p_CD225int_CD127p_Tmem
SE_18006chr19:1854567-1858438CD4p_CD25-_CD45ROp_Memory
SE_20207chr19:1854775-1857036CD56
SE_20207chr19:1857073-1858104CD56
SE_20804chr19:1851994-1859364CD8_Memory_7pool
SE_22514chr19:1854652-1858255CD8_primiary
SE_23274chr19:1855536-1863748Colon_Crypt_1
SE_23831chr19:1855456-1863700Colon_Crypt_2
SE_24756chr19:1851482-1865735Colon_Crypt_3
SE_27152chr19:1853176-1865991Esophagus
SE_34338chr19:1852133-1866086HCT-116
SE_41602chr19:1854125-1856964LNCaP
SE_41602chr19:1857007-1862712LNCaP
SE_45211chr19:1855501-1858228NHLF
SE_50407chr19:1852750-1865843Sigmoid_Colon
SE_52963chr19:1854521-1862878Small_Intestine
SE_53592chr19:1853107-1866012Spleen
SE_57652chr19:1857385-1857987VACO_503
SE_61842chr19:1851542-1865663Toledo
SE_68584chr19:1847293-1885536TC71
SE_68585chr19:1847293-1885536TC71
SE_68586chr19:1847293-1885536TC71
SE_68587chr19:1847293-1885536TC71
SE_69023chr19:1852746-1858528H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1918568731857008
Enhancer Sequence
GAGACGGCGG GAGGGGCACG GCCATGCTCA GGGTGACCGA GTGACATCTC TGCTCTAAGA 60
TCAGGGGCTG CCCTGGGGAG CCCAGCTGAG GAGGGGCACG GGAGGGTGGA GGGGTCTGCC 120
CACTGAGGGG CACCAGCGAT CACCCGTGAC CCAAGAAGAG CTGGAAGAAA AAACCTTCCC 180
TTCTCATCTC ATCCTTCCTC CCTGCCACAC CCCGACACCC TCAGCAAAAC AAGACTGCAG 240
ACAGAGACCA GCAGCCCCCC TCCCCAAGAG GTTGTGAATC CAGGCAGCTG GAGAGGGGGA 300
GAGACCAGCT GTCACCAAGA CCAACAGTAG CCTCAAATCC CTGGGGCTGC CTGCTCCACA 360
CCCCAAGTCT CCCCCAAGCA ACCCAGGATG CAGCTGGGGT CGCGGGTCCG CCCCAGCTGG 420
GGGCCGTCTA CAACCCAAGC AAGAGGCGCA GAGCAGCCCT GGAAGGGACC CCACTCCCAT 480
CTCAACCACT GGGCCCTGAC AGCTCCCAAG GGCCTCAGTC TGGGGACGGG GTCTGGCTGT 540
GGGAGCGCGG CTGGAGCAGA CCACGGGATT GGGGCTCGCG CCCCTCCAGG GAACATGCCG 600
CCGTGTCGCC ATCTTGCAAG GCACAGGCGG GGAGGCGGCA GGAGGGAAGG GGGAACATCC 660
CACGGCTGGG TGCCGGACAG TCAGTTGGTT CACTTCCCCT TTCAGGGCGG CGGGGCTGGT 720
CTCCACTCCC TCTCCCCCAG TTCCACTTTG CAAGGAGGAG CAGGTTGCCG GGGTGGGGGG 780
GGCGACCGGG GCAGGGGCGC GCAGCCGCTG GGAACACAGC TGCCGCACGT AGCTCGGCGG 840
CGGCGGCGGG GACATCCGCA GCCCCAGCCG GCCCCGCTCA CGTGGTCCCA CTCCCGCCGG 900
GGCCAGGGGG CCCGGGCCAG GGTCGCCTCT CCGGCCTGGG TGCCTGCCAG CCCCGCCCCG 960
CGCTTGGAGA CTGAGGCGCG CACATGCGCA CGTGGGTGGC GGGGCAGGGG GTGCACGGGC 1020
TACCCACCCA CGCTGCGCTG GGCGAAGCGC CTCTGCGAAA TGCCAGGCCC TGCCTCGCAC 1080
ACAATCCACT CGCAGGGAGG AGGGTGGGGT GAACTTGTGG GGGCCCAGAG CGCGCTGCTC 1140
CTAGCCAGCC GGGCCCCCAG GTGCACAGCC ACCCAGCTGC TCCGCGCTAC CTGGCCGAGA 1200
CGCAGCGCCC TGAGGATGCG GTGGGTGGGG ACAACGCGGG AGGGCAGTGT GGGCGGGGCC 1260
GCGGTGGACT TGACCCTCTG ACTCAGGCTG GGCCCGGGTG AGCTCAGGAC AGCCTCGGAA 1320
ACAGGCAGGC TCAGAAAAAT GGAGTCCAGG AAGTCCTGGA AACCTGGCCC GGCCCCGTCT 1380
GAGCCGGCAC AGGAGGGGCC TGGAGACAGG ACTGCGGGAC TGTGCCAAGG GCCCTGGTTC 1440
CGACAGGGAA GCCTCACCTC CTGAGCTTGT CTGGGGGGCC TTGGGGTGGG GAGGGGGGCT 1500
GTGGCCGGCT GCCTGCCGGG GCACTCACGT CCACCTAACA GGTGGGGTCG GGTCTGTAGG 1560
GGAGGGCACA GGTGGGGAAG ACCAGCCCCA GCCGCAAAGC AAGCATCCCA GGAGAGCCAG 1620
GAAAGGCTGG GGCTGGGGAG GCCTCTTACC CACCCAGGGA AGGGAGGAGC TCCTGAAGGT 1680
GATCCTTGAG CAGGTTCTAT AGAACCTATA GGCAGCTGCT TCTGGGAGCC GCTGCAGAAA 1740
AGGGGGAACA CTGGTGGTGA GGCCCTGCCA GCCTGGGGGT GGGGTCTCGA ATACTACTGG 1800