EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS068-02699 
Organism
Homo sapiens 
Tissue/cell
GM18526 
Coordinate
chr19:1855260-1857560 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs74401481chr191855583hg19
rs10411759chr191857297hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:1856368-1856386TCATCCTTCCTCCCTGCC-6.08
EWSR1-FLI1MA0149.1chr19:1855390-1855408GGAAGACAGGCAGGAAAG+6.43
KLF5MA0599.1chr19:1857129-1857139GCCCCGCCCC+6.02
KLF5MA0599.1chr19:1855444-1855454GGGGCGGGGC-6.02
SP1MA0079.4chr19:1855422-1855437AGGGGGCGGGGTCTC-6.27
SP4MA0685.1chr19:1855420-1855437GGAGGGGGCGGGGTCTC-6.4
SPIBMA0081.2chr19:1856870-1856882CACTTCCCCTTT-6.07
ZNF263MA0528.1chr19:1856360-1856381TTCTCATCTCATCCTTCCTCC-6.11
ZNF740MA0753.2chr19:1856952-1856965GTGGGGGGGGCGA-7.04
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_05653chr19:1854545-1857986Brain_Cingulate_Gyrus
SE_12493chr19:1855582-1855832CD34_adult
SE_12493chr19:1855977-1856280CD34_adult
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_57652chr19:1855522-1856323VACO_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
AAAGGCTGGG TTAAGGGGGT ACAATCATGG CAACCTCCCT AACCCTCCTG GCCCCTCCAC 60
GAGCAAGGGG GCATGGGAGG AACCCGCAGG CACAGTCAGT CTGGGCCCCG ATCTCGGGGT 120
GTGGTTAGAT GGAAGACAGG CAGGAAAGCT CACAGGGAGG GGAGGGGGCG GGGTCTCCCG 180
GGAAGGGGCG GGGCCCGGCG GGCTGGACTC GCCCCACCCC CACGGGACAG ATGGCGCTGG 240
GCAGGGGCGG GCCACCACCC GGCCACTTCC TCCACAGTCC CCTCCCACCG CCAAGGCCGG 300
GCCTCGCCCA TCCTGCCCCT AACCAGCCGT CACCATCTGG GCCTGCCTGT GCGCCTCCAG 360
GCGGTGTGGG TCTTTGCTCT AGAACTGTGC CACCCGACCC CTTCCTTTAG CCGGGGTCTC 420
ACGCCCACAG CATGTGGCAT CGTGATGTCA GCGTCTCCCC AGCAGATAGG GGTCTCCAAC 480
GACTGGGGAG GGGCAGGTCA GTCCACCTCC ACCCAGGGAC CGAAGCAGGA CAAAGGGCCC 540
TGCATCCCCG AAGCTCCCAC CCTTTCGGGC CCTGCACCAG GTACCCTGGA CCCTGGCATT 600
CCGGGACGTT ATTCCCGTGA CACCCCAGGG TGGGTTGTGT GGATGGAGAC CGGATGTGCA 660
TGCCCCTCGT GGCACTGGTT GGAGCCCTGA GTAGCAAAAG AGACGTCAGA ACCAACTCCC 720
CTGAGTGGCC CCAAAGCCTA TTCTCAAGGA AGCCACAGCA GGGCCAGGAG GGTAGTCACC 780
CGGTGGGTTA CAAACTGGGC AGCCCACGCC CAGCACTGGA GGTTGCTCTG GCCCTGGGAG 840
CACTCCCACC GGTCCATGAA GAACTGCAGC CAGCCAGGGG CCTAGAAGGA CCCACAGCAG 900
GGACCATGGT GAGGGGTACA GAGACGGCGG GAGGGGCACG GCCATGCTCA GGGTGACCGA 960
GTGACATCTC TGCTCTAAGA TCAGGGGCTG CCCTGGGGAG CCCAGCTGAG GAGGGGCACG 1020
GGAGGGTGGA GGGGTCTGCC CACTGAGGGG CACCAGCGAT CACCCGTGAC CCAAGAAGAG 1080
CTGGAAGAAA AAACCTTCCC TTCTCATCTC ATCCTTCCTC CCTGCCACAC CCCGACACCC 1140
TCAGCAAAAC AAGACTGCAG ACAGAGACCA GCAGCCCCCC TCCCCAAGAG GTTGTGAATC 1200
CAGGCAGCTG GAGAGGGGGA GAGACCAGCT GTCACCAAGA CCAACAGTAG CCTCAAATCC 1260
CTGGGGCTGC CTGCTCCACA CCCCAAGTCT CCCCCAAGCA ACCCAGGATG CAGCTGGGGT 1320
CGCGGGTCCG CCCCAGCTGG GGGCCGTCTA CAACCCAAGC AAGAGGCGCA GAGCAGCCCT 1380
GGAAGGGACC CCACTCCCAT CTCAACCACT GGGCCCTGAC AGCTCCCAAG GGCCTCAGTC 1440
TGGGGACGGG GTCTGGCTGT GGGAGCGCGG CTGGAGCAGA CCACGGGATT GGGGCTCGCG 1500
CCCCTCCAGG GAACATGCCG CCGTGTCGCC ATCTTGCAAG GCACAGGCGG GGAGGCGGCA 1560
GGAGGGAAGG GGGAACATCC CACGGCTGGG TGCCGGACAG TCAGTTGGTT CACTTCCCCT 1620
TTCAGGGCGG CGGGGCTGGT CTCCACTCCC TCTCCCCCAG TTCCACTTTG CAAGGAGGAG 1680
CAGGTTGCCG GGGTGGGGGG GGCGACCGGG GCAGGGGCGC GCAGCCGCTG GGAACACAGC 1740
TGCCGCACGT AGCTCGGCGG CGGCGGCGGG GACATCCGCA GCCCCAGCCG GCCCCGCTCA 1800
CGTGGTCCCA CTCCCGCCGG GGCCAGGGGG CCCGGGCCAG GGTCGCCTCT CCGGCCTGGG 1860
TGCCTGCCAG CCCCGCCCCG CGCTTGGAGA CTGAGGCGCG CACATGCGCA CGTGGGTGGC 1920
GGGGCAGGGG GTGCACGGGC TACCCACCCA CGCTGCGCTG GGCGAAGCGC CTCTGCGAAA 1980
TGCCAGGCCC TGCCTCGCAC ACAATCCACT CGCAGGGAGG AGGGTGGGGT GAACTTGTGG 2040
GGGCCCAGAG CGCGCTGCTC CTAGCCAGCC GGGCCCCCAG GTGCACAGCC ACCCAGCTGC 2100
TCCGCGCTAC CTGGCCGAGA CGCAGCGCCC TGAGGATGCG GTGGGTGGGG ACAACGCGGG 2160
AGGGCAGTGT GGGCGGGGCC GCGGTGGACT TGACCCTCTG ACTCAGGCTG GGCCCGGGTG 2220
AGCTCAGGAC AGCCTCGGAA ACAGGCAGGC TCAGAAAAAT GGAGTCCAGG AAGTCCTGGA 2280
AACCTGGCCC GGCCCCGTCT 2300