EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS113-10608 
Organism
Homo sapiens 
Tissue/cell
Keratinocyte 
Coordinate
chr13:100033210-100036490 
Target genes
Number: 12             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9557207chr13100036418hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr13:100033819-100033837GGAAGGAAGGCAGGCCAG+6.45
SREBF1MA0595.1chr13:100034949-100034959ATCACCCCAC+6.02
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_10213chr13:100032758-100034087CD19_Primary
SE_10213chr13:100034387-100035795CD19_Primary
SE_11028chr13:100021349-100036804CD20
SE_11845chr13:100032468-100037699CD3
SE_15478chr13:100032613-100035519CD4_Memory_Primary_8pool
SE_15478chr13:100035656-100038682CD4_Memory_Primary_8pool
SE_15816chr13:100032589-100038838CD4_Naive_Primary_7pool
SE_16353chr13:100032502-100034248CD4_Naive_Primary_8pool
SE_16353chr13:100034289-100037293CD4_Naive_Primary_8pool
SE_16919chr13:100032844-100034083CD4p_CD225int_CD127p_Tmem
SE_16919chr13:100034191-100037834CD4p_CD225int_CD127p_Tmem
SE_17308chr13:100031714-100041307CD4p_CD25-_CD45RAp_Naive
SE_18493chr13:100032105-100041266CD4p_CD25-_Il17-_PMAstim_Th
SE_19593chr13:100032782-100039370CD4p_CD25-_Il17p_PMAstim_Th17
SE_20213chr13:100032074-100037188CD56
SE_20908chr13:100031873-100036031CD8_Memory_7pool
SE_21470chr13:100032320-100037739CD8_Naive_7pool
SE_21952chr13:100032543-100040670CD8_Naive_8pool
SE_22658chr13:100032195-100040441CD8_primiary
SE_50911chr13:100032443-100034312Sigmoid_Colon
SE_50911chr13:100034387-100037802Sigmoid_Colon
SE_52942chr13:100032590-100034334Small_Intestine
SE_52942chr13:100034344-100036565Small_Intestine
SE_62301chr13:99990726-100041194Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr13100035732100036024
chr13100033242100033451
chr13100034200100034294
chr13100034563100034616
Number: 1             
IDChromosomeStartEnd
GH13I099379chr13100032154100037167
Enhancer Sequence
CGCTGCAAGC TGTGACAGCA GACGCTCTCT TCTGCCAAGA CCTGTGAAAA GCCAGTCTTA 60
GTTGTCAAAA CCAGCACCGC GGCACATGTC GTTCATGTCT GAGAGAATGA ACTCAGAAGG 120
AAGTCTCGTG TACATAGAAA GCTTTCGTTC TTACTCTAGG ATGTCACCTA CGTGACTTAC 180
AACCCAGCCC AGCCATCCCA GACCTAAGGG GTTCTTCCCT CTCCAGGGCA GGGCCTGCAT 240
GCAGTCCATG CTGCTGCCCT GTGTTGGTGA CCTGTGTGTA GCCAGCCCAT TATCAGCATC 300
CTGTGGATTC CAAACCAAAT GTATCATCAG TGGAGGGAGA GCTCAAGTGC CAGGTGGAGC 360
TGTGGCCTAA AGTCACACTT CATCACTCCA GATTATGAAT CGTCATTTGC CAGATCTCCA 420
AATTGCTGAG TGTGGACAGC AAATGGATTC GTTTGTGCTG GCTGGGTGCA AAGAAGCAGC 480
CAGTCCTCAG CTGCACTTGA AGTACTACAG GTAGTAGTAA AGGTAGCTTT TCCAAGCCGT 540
TTAAATAAAC GTCATTAAGA GTGGCCAAGT TGTTTGGGGG CCATGGCATC ATGGTGGTGG 600
ATAGTAGGTG GAAGGAAGGC AGGCCAGCTC CCGTTTGGCC TGAGTTATCT CCACCAATGA 660
CAATGGTCCT TAACTGGAGG GAACATCATA CAGGTTATTT CCACCCAAGA TTGGAAAGAC 720
CACCTTGATC AGAGAGAGTT TTCCTTCCAC ATGACACATA TCCAGCCTGA GTCCTCCAGC 780
CCCTCTCCCT GCACAACCTG ATGGAGGCTT GAGAAAGCAC AGGGAGGAAC ACTTAGCTTG 840
AAAATGTTCC TAAGGAAAAG GAAAGTGTGA ATTCTGAGAA CCAAGTGGCA GAATTGAAGT 900
TTCACATCTG GCAAAAGCTT AAACAGATTA TTATCAAATA GATGGTTTGT GAACGTTGAA 960
AAGACAGCTG TGGTCTAGGA CACCAAACCA ATCCTGTTGG CAAGAGATCA CCAAGACCTT 1020
TGACAACATC TCATCAGCTT ATGAGAGATG TTGGTGACAT GCAGAATGGA TAATGATAGT 1080
GCAATGAAGT GGGTTTGAAA CTGATTAAAA ATGTTGATTA ACCCCTTGAA CACAGAGTTC 1140
TGGGCTCTTT GACCTGACGT GTTTGACATT TTCATCAATA ATAACTTGAA CAAAGTTGTA 1200
GAGGTTTACT AATCAAATTT AGGCATGATA CAAGTTTGAG GGAGATGATT AACAGTAGAT 1260
AACAAAATGA GAATTGAAAA TAATTCATTT TGGTTGACTG GAAAATGATC AGATGGAATT 1320
TAACAGAGAT ATGTAGAGTC CTAGACTTAA AAGGTCAGGT AGGATTTGAG AGACCTGACT 1380
TGACAGCATT TTATGTGAAA ATTCCTGAGT GTTTTCAGCA GGCCCAGCTT AACTGGCCAC 1440
ACCAGTGATG CAGCTCCTTA CACAAGTGCA TGCACAGGCA CACACAACAC ATATGCACAC 1500
TACTAATGCA TTCCTCTGCT CTCATTGAAG CTAAGGGCCC AGACTGTTGG AGGGCAGTGG 1560
CCTCACTGCC CTGGTGAGAC CACACCCGTG GTGTCACACT CAGTTCTGGG CGCGGTGTTC 1620
TGAGACGGTG TGCACAAATG GGAGGGGATG GGCTGAAAGG AACTGGATCC TGAAACACAG 1680
GAATGAGCAA AGGCAGCCAC AGCCCTCATA CTGGGAGTTC ACAGTGGTGG GGAGAAGCTA 1740
TCACCCCACA GACACAGCTG CAGGGAGCCC AGGACAGAAG GCAGTGGGGC AATGAGGACT 1800
TCGCTCTGGG GGCCTTCTAG TCTGGGAGAC ATGGAAAAAG GCAGGGGCCC CAAGACCCAC 1860
CAGGGGAAGA GGAGTCATCA GGCTCAGGGC AGAGGGCAGA GACAGCAACA CAGCAGAACA 1920
AGCCACGGTA CCCACAGGCC TGGGTGGGGG CCGAGAAAAG CCAGTGGGTT GAGGGAGGAA 1980
GGAGAGGGCT GTCACACCCG CAAAGTGCTT TATGTAGGAA AAGAGAATAG GGTTGTTCTC 2040
GGTTACTTCA AAGGGCAAAA TCAAGAGCTG TGGCATTGTG TGGATGGCAG CTTGTGAGGG 2100
GCAGAACACC AGGGTGGCAG CATTCTCAGC CACCTGGCAG TGAGGCCAGG GCACTCAGCC 2160
ACAGCTGATG TGCATATGAT GCATTAGTAG TGTGCATGTG TGTGTGTGTG CCTGTGCACG 2220
CTCTTGTGTA AGGAGCTGCA TCACTGGTGT GGCCAGTTAA GCTGGGCCTG CTGAAAACAC 2280
TCAGGAATTT TCACATAAAA TGCTCTCGAG TCAGGTCTCT CAAATCCTGC CTGACCTTTT 2340
AAGTCTAGGA CAGTACATAT CTCTGTTAAA TTCCATCTGA TCATTTTCCA GCCAACCAAA 2400
TGAATTCTTT TCAATTCTAG TTTTGTTAGC TACTGTTTTT TGTTTTTTGT TTTTTTTATC 2460
TACGACACTC TCTCCTCTGG TGGGAAAACA AACTAGAAGG TTTCTGCCTT TGCTCTACGC 2520
TGTCCACCAG CCCTGGGCAG CTGAGCATGA ATCACCTGAG GGCGCCATAG TGTCCCAGGT 2580
GCTGGGCATC TTGCTGCTCC AGGACAGCCC TCCCCACCGC AAGGCATTTG GAAGACACCT 2640
GGCAGCCCTT CTTGGCTTCC TAGCCAGGGC TGTGCGTCAG TCCCCGTGCT AAGGGTTGAA 2700
AGCAACGTTC CGGGGAGGAG CACGCTCACT GCGTGCATTT GTAAGCCTAG TCCTCACCCA 2760
CTGAGTGGTC CCATGACATG GGCGGCACCC CCCGTTTGGA AAAGCCCTGG CTGGACTCCA 2820
GCTTCTGAGC AGTGTCCACT GCGTGTCCCT GTTGGCCCTC AACTCTTCCC TAAGGCTTTT 2880
GGGGGAGGAG GGTCTGGGTG TCTGGGCCTG GGTGGTCACT GGGAGGTTCC CTCCCCCACC 2940
TGCCTCTCTA CTCTCTGCAC CTTCTTCCTC ACCTTGCTGA GTCCTTAGGT TAATTTTGCT 3000
CAGAATATCC AGAGTTAGCC ACTAGGCTGC GGGTGAAGTG GGATAGAGAG GAAGAACAGC 3060
AGGCTTTCTG GAGCCACATG CCCAGGCCCA TGCCCGGCCC CTCCTCCAGC CACCCCATGC 3120
CATAGTCCCC ATTCACACCC ACTGAGTCCC CTGAGCAGAG GAAGGGGTGG TGATACTGGG 3180
CCCCTTCTCT TTCCACCATG TAGCACCAAG TAGCTCGCTC TCTTTCGGAA AGAAAAATTG 3240
GAAACTCTGA CTAAGTCCTC AGGTGAACCC ACAAAAGCCT 3280