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

TagContent
EnhancerAtlas ID
HS180-04025 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:198589580-198591980 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ETV6MA0645.1chr1:198590193-198590203CACTTCCGCT-6.02
ZNF263MA0528.1chr1:198591116-198591137GAGGGAGGGGGAGAGAGAGAA+7.16
ZNF263MA0528.1chr1:198591112-198591133GAGGGAGGGAGGGGGAGAGAG+7.35
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_09213chr1:198588981-198592120CD14
SE_10200chr1:198588027-198594672CD19_Primary
SE_10874chr1:198579403-198671825CD20
SE_11822chr1:198587521-198595241CD3
SE_13336chr1:198589295-198591554CD34_Primary_RO01536
SE_14382chr1:198587909-198593024CD4_Memory_Primary_7pool
SE_15405chr1:198587286-198591751CD4_Memory_Primary_8pool
SE_15805chr1:198588242-198592643CD4_Naive_Primary_7pool
SE_16283chr1:198588465-198591973CD4_Naive_Primary_8pool
SE_17305chr1:198587675-198600249CD4p_CD25-_CD45RAp_Naive
SE_17776chr1:198587525-198598559CD4p_CD25-_CD45ROp_Memory
SE_18245chr1:198586009-198601808CD4p_CD25-_Il17-_PMAstim_Th
SE_19200chr1:198588420-198594418CD4p_CD25-_Il17p_PMAstim_Th17
SE_19995chr1:198587255-198594711CD56
SE_20746chr1:198588472-198591608CD8_Memory_7pool
SE_21924chr1:198588052-198594703CD8_Naive_8pool
SE_22285chr1:198585323-198601107CD8_primiary
SE_31026chr1:198588235-198592906Fetal_Thymus
SE_39433chr1:198589254-198591591Jurkat
SE_39433chr1:198591613-198593060Jurkat
SE_49861chr1:198588569-198593134RPMI-8402
SE_58290chr1:198564715-198671046Ly1
SE_59080chr1:198588455-198654514Ly3
SE_59608chr1:198585244-198671628Ly4
SE_60444chr1:198588133-198656098DHL6
SE_61004chr1:198588339-198656148HBL1
SE_61429chr1:198565046-198658062Toledo
SE_62210chr1:198565497-198666528Tonsil
SE_66263chr1:198589254-198591591Jurkat
SE_66263chr1:198591613-198593060Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1198590109198590618
chr1198591244198591462
Number: 1             
IDChromosomeStartEnd
GH01I198617chr1198586995198595024
Enhancer Sequence
ATACTTCCTC TTCTATTTGA AAAGTGTAGA TTTACTTACA TTCTTTTAAA TATATCAGCA 60
CAGACTATCA GGCCGAGGAT CACTGTCTTC CAACACAGTA AACATGGACC TGGTTCTTGT 120
GCTCCAGAGA AACAAATGAA AGAGCAGGCC TCAAGGAATT TTGTTCATTG GGATCAGTGG 180
GATCACAAGT ATAGATCTAA AGAATGGAGT TCCTTCAGAG CTCACTTCAG GTGGCCAAGA 240
TGAAAATATG TACTTTCCTT CATAATATAC TTAAGAAGAT AAGGTCAGTT TTGTCATTGA 300
TCTGGTCCTA TTCACCTTGT TTTTCTCTCT TAAATTATTT CTTTACCATT GTGGAGATAA 360
TCAACCGCAT GGTGTCATCA CTCATTTATC TCTAAGCATA ACAGACATTT TCAACCCATT 420
TCAGGTGTCC TCAAATTATT CATTTTTTAT TTAAATGAAG AATTGTCCAG AGTTAGCATG 480
TAAATATTAG CTAAGGGCAG GATGTGTGTG TGTCATGGAG GGGAGGACCT CTCCTGTTTA 540
GGAGGAACTG CTGGCCCTAA TATGCATGTC ACATACATAT GAACCTTGAT CGGCTGTCAT 600
GCGGAAGGAA TTACACTTCC GCTGGCCTCC CCTACCACAA CCACAGGTGG AATCTAAGCT 660
AGGCACTGAA CTTGGCTCAC ACAGCTGTGA GCTTGCGCTG AGTCTCATCC TTTGCTGTGG 720
AACTCCCTCT GCTGCTTCCT GCCCCAGCAA ACTCCCCTCT ACCCAGCCAC TGGAAAGGAG 780
TCCCACAGGA GGGGAGGGAC AGTAGAGTAG AGCCCAGCTT CTCTGTCCAA CACATAAAAG 840
CTCTGAAAGG CAGTTATAAA AGGCTGAACT GGGAGCAGGT ATTGTTAAAA AGGGAACCAC 900
TGACTTCCTG TGAGCACATG TTCCTGTCTC ACTCTTGCTC TGCAGCACAG TAGAGGCTGT 960
TTAGTTCATC ACAAAGGAAG TGCATCAGCA CTCCTGAAGA TGCTACTCTA AGGGCACCTT 1020
TGAGTTGTGG GCCAGGAAGG CATTCCATAG TAAGACGAAG GAAAGGCCAA GTTCCTATTG 1080
TTAGCGTCAC TATGCTTCTG GTTTTATAGT TTCCTAAGTT ATTGCCACAG GTCATGGATC 1140
TGTGGCGCTC AAATGTTCGC TCACAAGGTT CACAGCACAT TCTTTGCAGT TGCACCACCC 1200
AGCTAGGAGG GGCGAAACCA ATGGAGCATT TTAGGCAGAG CTCATTTCCG CCCACATCAA 1260
AAGTAAGAGA GAAGTTTGTG GAGAGCTACA TTTGAGCCCT CCATTAGCTG TTTTACATCT 1320
TGTAGGCCAA GGTGACACTT TCTACACTAT GTGCTGGTGA GATACCACAT GGACAAAATG 1380
TTGTAGAGGA CCCAGCCTGA AAAATGCTCA GGCTTTAAGT CTGAGCAATC TCCACCACAT 1440
CTCTACTCCA CATCCCACCC CTCCTGGAAT TTTAAGTCAG GAGACACATT GTGAGTGCAT 1500
GGACAAAATA AAGAAAAGAA AGAGAGAGAG AAGAGGGAGG GAGGGGGAGA GAGAGAAAAA 1560
GTATATCAAT TAAAAGTTTG CTGAAAGAGT CATGACATAA AGAAGATGAA AGAAAAAAAC 1620
AAATTAGATT GTTACCAAGC TGTACATTCT TTGTTGAGGG AGAATAGAGA TGAATTGGTA 1680
GCAGAGAGGA AGAAAAAGGA AGCATTTTAA GATGCAAAAC AGGAGAAATC AGACTTAAGC 1740
AAGAATGGAG AAATAACTAC ATTTATCCAC ATCAGCTGTA TCTTACCAGT TTGACTACTC 1800
TAAATGCTTG GGGATAATCT GGGAGTTTTT CACTGCTCCC CTCCTGCTGA CAGTCCCAAA 1860
CATATTGATG AGGCATTTTT AATAGCTTTC ACCTCTGGCT CCTACTACAG CTTCATGTCT 1920
TTTTCCTTGG TTCTTATCCT CATCGTGGTG TCATGATTAT TGTCCTCTCA GTCAAGCCCA 1980
TCCTGTGCTA CTGACTGAAT GATTTTTATT AAAAATAAAT TTTCCCCTAT GCCTCTCCTG 2040
CTTACAATGC CTTATGATCC TTGATTGCTC ACAGATTGAA ATCCAAATCT TTGAGGATCC 2100
CATTCAAGAT CTTTCAGTGC CTGAGTATAG CTCGTCTCTC CAAATTCTTC TTCTGCATAT 2160
TATGTGCCTG CTAAAGAAAG TACTTACAGT TGTTCAAATG AGATGTTTCT TTTGGAAACC 2220
TCCCTGCATT CCTACCTGCT AACCCCCTAT TTGGAAGTTA ATTGTTGTCT TCCCCCACTC 2280
AGCTCACAGG TGTCCCCTGT GCACCTTCTA CTGCCCACTC AAGCATAGTT GATCACTTCC 2340
TCCTTTAGGT CTCAATGCCA TGACAATTTA ATCACACTCC ATTTTCATTA TTTTTTATAA 2400