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

TagContent
EnhancerAtlas ID
HS031-09231 
Organism
Homo sapiens 
Tissue/cell
Denditric_cell 
Coordinate
chr16:81531640-81533900 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56823429chr1681533789hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:81533878-81533896CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr16:81533882-81533900CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr16:81531913-81531931CATTCTCTCCTTCCTTCC-6.77
EWSR1-FLI1MA0149.1chr16:81531917-81531935CTCTCCTTCCTTCCTTTC-7.64
EWSR1-FLI1MA0149.1chr16:81533842-81533860ATTTCCTTCCTTCCTTCC-9.03
EWSR1-FLI1MA0149.1chr16:81533854-81533872CCTTCCGTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr16:81533870-81533888CCTTCCGTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr16:81533846-81533864CCTTCCTTCCTTCCGTCC-9.17
EWSR1-FLI1MA0149.1chr16:81533862-81533880CCTTCCTTCCTTCCGTCC-9.17
EWSR1-FLI1MA0149.1chr16:81533850-81533868CCTTCCTTCCGTCCTTCC-9.35
EWSR1-FLI1MA0149.1chr16:81533858-81533876CCGTCCTTCCTTCCTTCC-9.35
EWSR1-FLI1MA0149.1chr16:81533866-81533884CCTTCCTTCCGTCCTTCC-9.35
EWSR1-FLI1MA0149.1chr16:81533874-81533892CCGTCCTTCCTTCCTTCC-9.35
EsrraMA0592.2chr16:81532865-81532876CTCAAGGTCAT+6.02
EsrrgMA0643.1chr16:81532866-81532876TCAAGGTCAT+6.02
HEY2MA0649.1chr16:81533198-81533208GACACGTGCC+6.02
Npas2MA0626.1chr16:81533198-81533208GACACGTGCC-6.02
Stat6MA0520.1chr16:81533298-81533313GGCTTCCTGAGAAGT+6.33
ZNF263MA0528.1chr16:81533692-81533713TCCTCTTTCCCTCCCTCACTC-6.34
ZNF263MA0528.1chr16:81533850-81533871CCTTCCTTCCGTCCTTCCTTC-6.39
ZNF263MA0528.1chr16:81533866-81533887CCTTCCTTCCGTCCTTCCTTC-6.39
ZNF263MA0528.1chr16:81533846-81533867CCTTCCTTCCTTCCGTCCTTC-6.62
ZNF263MA0528.1chr16:81533862-81533883CCTTCCTTCCTTCCGTCCTTC-6.62
ZNF263MA0528.1chr16:81533878-81533899CCTTCCTTCCTTCCTTCCTTC-6.94
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_09239chr16:81529931-81532741CD14
SE_09239chr16:81532844-81537999CD14
SE_11291chr16:81532822-81542648CD20
SE_23105chr16:81531096-81532058Colon_Crypt_1
SE_23862chr16:81531063-81532264Colon_Crypt_2
SE_26527chr16:81530858-81532243Esophagus
SE_26527chr16:81532504-81534038Esophagus
SE_31484chr16:81531071-81532101Gastric
SE_35877chr16:81530694-81535589HMEC
SE_42333chr16:81530117-81532266Lung
SE_52343chr16:81524595-81532175Small_Intestine
SE_53457chr16:81530078-81531871Spleen
Number: 2             
IDChromosomeStartEnd
GH16I081497chr168153060781532004
GH16I081499chr168153268581540040
Enhancer Sequence
TCATGCATGC ATGTGTTGGT TCATTCATTC ATTCTCAGAG TACCATGGTG GCTCTGAGGA 60
CAGAGGTCAG ACCCAGCTGG GTTGGAACCT GCTGCTCCCT AGCAGTGGGC CTCTGGGCAG 120
ATGTTTTAAC CATAGAACTC GGCTTCCTTG TCTGAAAACG TGGCTCCTTC TAGGACAGTC 180
AAGAAGGTTC AATGAAATGA TGGATGTGGA GCCCCAGGAC GTGACCTGAG GATGGTGCTT 240
GTCATGTTGG GGTCTGTGTC CCTCCCTTGG GCACATTCTC TCCTTCCTTC CTTTCCAGCT 300
TCCTGAGGAC GGTCCAGTGC CGGGGGCTGG GCACAGGCCT GAGTGAGATG CGGCCCTTGT 360
CCCCCGGCCT TTTTGGTCTG GGTCCTCACC TCTGCACCGA GTCCCCCTGG GGCTGCTCGG 420
CAGCTCTGAG GGGGCCACTC TGCCTCTGCC CAGTGGTCCT GCTTTCTCAC GGGGGTTATC 480
AGGCCTCTGC TCCTCGCGCC TCACTCTGAG AGGGTCCTTC CACCTGACTC ATGGCTCCCA 540
TCCCTCCATG CCCCTGCCCA GGTGCCCACA CATGTGTGCC CCAGAACATG GCTGCACACA 600
CTTGCATACC CCACGAGCAC ACACGTGTGT GCATGCATAC ACCCCATGGT CCTTGAGCAC 660
ACATGTCCTG GGCCCTGGCA TGCACTCCCC CAGGCGTCAT GTATACACAC AGTCCACACG 720
TTTGCAAACG GGCAGACACA CCTCCCTCTT GCACATCCGT GCACACCCAG CCCATATCTT 780
CCTGCCCCTG CGTGTGCACA CAGTCCCAGT TAGTTTACAC CGTGCACACC TCTCCATACA 840
TACAGGTTCC CAGCTGTGCG ACCACTCACC CACACGTATG CATTTATTTT TTAACACACA 900
CATGCATACC ATTTAGTAGG ACCCCATGTA CAAGCATCTG AGTGCTTTAC AAATTCAAAT 960
GTATTTAATC CCCCTATCAA CACTAGGAGG TAGTTTCTGT TATTAGCGCC ATTTTACAAA 1020
TGAGGAAACT GAGGTGTAGA GCAGTTAGAT CGGTGTAGAG AAGCTAGATC GTGTGCTCAA 1080
GGCTTCAGTC CAGGCTCTTG GCCCTGACAC GATGCTGTTT GCCTGTTGAA GATGTGTGTG 1140
CATGCATGCA CCATTCACAC TGTGAACGTG TCCCAGCATG GCCACACCCC CTCACCGTAT 1200
ACACATATGG CCATGAGCAC TCAATCTCAA GGTCATGGAT GCACATGCCT CACACCTATG 1260
CATGGAAGGA CACTCGGCAC ACATACTTGT CTCTGCACAC ACACACCACT TGCACACCCA 1320
TGTACACATG TGCCCCAAGC CTCGCCCCAA TCTCCAGCTC CCTTTCAGAG TCCCTTCTAG 1380
GATATTCTCT GATTTCTCCC AAGTGCCCAG TTCGGGAGGG AAGTGACTGC ACAGATCTGG 1440
ACCTGGCGAT GACCTCTGAG TGGGAGGCAG CCCTGGCTGA GCTGTCTCCT CACCTTAGCA 1500
TCCGCCTGTC CCGGCGCCCA TGTAGCTTCC TTGTCATCCA TCTTCTGGGC TGGCCCAGGA 1560
CACGTGCCCC CATCCCAGCC TCCAAGAATC TGGGAATGTC CTTAGCAGAC TGGGCTGGCA 1620
TGTGGCCTCT GCCCGGGGAG CAGAGGTGGC TCCCCAAAGG CTTCCTGAGA AGTGGTGGAG 1680
GAGACTCAGC TTCCCCGTCC AGTCCTTTAC CCCTCCTTTA CCCAGCAGCG CCCTCTGAAT 1740
CTGAAACAGT TTTGGGGGCG GCAGCTCCGG TCCTGCCCAG CAACTCGCAG TTGTTGCCTG 1800
TGGCATTCAG ATTCAAGTCT GGGCTTGTCA GCCCGGGCGA GACTCTCCTA TTTTGGCCCT 1860
ATGGGAGGCA TCCAAACTCC TCTGCCCTTG CCTTCCGGGG CGCCCCACGC ACTCTGGGCT 1920
TCACCTGGCT CCTCTGCTTT GCTTGGGCTG CTGACTTCTG GAGGAGCCCT TTCTTCCTTC 1980
TCTCTCCTGA TGCAGAACAT ACCCAGTCTC CCTGGGGCAA TCGGCCTTCT TCAGCCACTC 2040
CTTGGTCTCT GCTCCTCTTT CCCTCCCTCA CTCTGTGTCC TGCCAGCCCC AGCCTCTGGC 2100
GACTTTTAGA GCTGGTGCGC AGTCCTGCCT GAGCATCGGT GAACATGACG CCATGGGCTG 2160
TGGCTTAACG ATTCTTTTGG TGAATTTTGA TTCTTTATCA AAATTTCCTT CCTTCCTTCC 2220
GTCCTTCCTT CCTTCCGTCC TTCCTTCCTT CCTTCCTTCC 2260