EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-11034 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr17:57924790-57927460 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs11332131chr1757926392hg19
rs112721625chr1757927427hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr17:57926011-57926023GTTTGTTTGTTT+6.32
ZfxMA0146.2chr17:57925752-57925766CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00167chr17:57921765-57927189Adipose_Nuclei
SE_10048chr17:57913237-57927649CD14
SE_18274chr17:57913216-57925634CD4p_CD25-_Il17-_PMAstim_Th
SE_23233chr17:57924699-57925649Colon_Crypt_1
SE_23233chr17:57925732-57927369Colon_Crypt_1
SE_24435chr17:57924806-57925507Colon_Crypt_2
SE_24435chr17:57925755-57926396Colon_Crypt_2
SE_25771chr17:57921970-57927112Duodenum_Smooth_Muscle
SE_27082chr17:57922837-57925640Esophagus
SE_27082chr17:57925703-57927556Esophagus
SE_27746chr17:57920340-57927032Fetal_Intestine
SE_28673chr17:57920322-57927067Fetal_Intestine_Large
SE_31691chr17:57922855-57928410Gastric
SE_32541chr17:57921468-57927090GM12878
SE_33772chr17:57913056-57927377HCC1954
SE_34288chr17:57912088-57927293HCT-116
SE_34651chr17:57912951-57927107HeLa
SE_37171chr17:57913355-57925459HSMMtube
SE_43382chr17:57912648-57925582MCF-7
SE_43382chr17:57925698-57928424MCF-7
SE_44187chr17:57913075-57925500NHDF-Ad
SE_45686chr17:57913234-57925367Osteoblasts
SE_47118chr17:57902074-57938709Panc1
SE_47932chr17:57924766-57925603Pancreas
SE_50387chr17:57924697-57925650Sigmoid_Colon
SE_50387chr17:57925686-57927577Sigmoid_Colon
SE_51624chr17:57921832-57925543Skeletal_Muscle
SE_52483chr17:57922815-57925637Small_Intestine
SE_52483chr17:57925694-57927477Small_Intestine
SE_54204chr17:57922884-57925577Spleen
SE_54204chr17:57925678-57927318Spleen
SE_55059chr17:57922569-57925554Stomach_Smooth_Muscle
SE_57301chr17:57924882-57925477VACO_400
SE_58037chr17:57924837-57925363VACO_9m
SE_59128chr17:57902596-57931450Ly3
SE_61214chr17:57902066-57937473HBL1
SE_62339chr17:57902123-57931675Tonsil
SE_64271chr17:57913695-57925402NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr175792483657925484
chr175792577657926127
Enhancer Sequence
TTTTTTTTTT TTTTTTAATA CAGAACACAA ATTTGAGTGT CATTCTTGTG CAGGGGCCAT 60
GCTAATCTTC TGTATATTGT TCCAATTTTG GTGTATGTGC TGCCAAAGCA AGCACCCAGC 120
TTCTTTTCAT TAGTTAAGAA GATGAAGGCC AAGACTAAGG CAGGGAGGCC TTTCTCTGCC 180
TTTCACTCTT TAGTGCACCT CACAGTCAGT TGCACTTGAG TAAGGACTGC TAAACCTCTC 240
TGAGAGCTGC CAGATGTTCC TGCCTAGCCT CAGGTTGTTG GTTCTTCAGA CACCTCTTCA 300
TTCTGCCCAT TGCACCAGCC CTTTCCCATC TCCATGTTCC CTCCATGGTA ATTTCTTTGT 360
ACACAACAAC CACACGGAGC ACCAGCAATC AAGATTAGCT CCCGGGAACT CTGGCGTGCC 420
CTGTACCAGG AAGCACAGTG GATTACTACA ACTTTTGATA ATGATTGTTT GCTTTGTACC 480
AGGCATTATT TTCAGGGCTG TTTCACATGT GTTGTACTTA ACAACCCCAT GAGGAAATTA 540
AGGCAGGGTG GTTCAGTAAT TTGTCAAGGG AAACAAGGAA GTAGAGCAGG CAGCAGAGGC 600
GTTCTGGCTC TGAACTACTC TGTTCTGTAG AAATCAGTGC AAAAGTCCAA GCTTCAGCAT 660
ACTTGTTTCA TCTTGTGATC ACAGGTAGTT TTTTTTGTTT TTTTTTTGTT GTTGTTGTTG 720
TTGTTTATTT GTTTGTTTTG AGATGGAGTC TCGCTGTCGC CCAGGCTGGA GTGCAGTGGG 780
GCGATCTCCG CTCACTGCAG GCTCCGCCTC CCGGGTTCAA GCCATTCTCC TGCCTCAGCC 840
TCCCGAGTAG CTGGGACTAC AGGCGCCCGC CACCTCGCCC AGCTAATTTT TTGTATTTTT 900
AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTC AATCGCCTGA CCTCGTGATC 960
CGCCCGCCTC GGCCTCCCAA AGTGCTGAGA TTACAGGTGT GAGCCACCGC GCCCGGCCCT 1020
GATCACAGGT AGTTGATGGA GAAAGGAAGA TAACAGAAAA TCAAGGCCAC AACCTCAAAT 1080
TTTGCTATTT AAATAGATAA GCAGACTTTA CTCTTCCCTG TATCACAGGG TTGGAAAAGC 1140
AAGCTCCATT CTTAGCCATC CATGTGGGCA GATTCCCAGA GTGGTGTTTG CTATAATTAT 1200
GATTTAAAAG CAAGGTTTTT TGTTTGTTTG TTTTAAGGAG ATGGGGTCTC CCATGTTACC 1260
CAGGCCGAAC TCCAACTCCT GGGCTCAAGT CATCCTCCCG CCTCAGCCTC CCGAGTAGCT 1320
GGGACTACAG GCACTCACCA CCACACTTGG GTAAAAGTAA TTTCTATTTC TACAGCCTTT 1380
TTTTATTTTT CAAAGTATTT TAATGTCTTG AGTTTGGGTT TTGTTTTGAG ACAGGGTTTC 1440
ACTCTGTTGC CCAAGCTGAA GTACAGTGGC GCAATCACAG CCACAGCTGA CTGCAACCTC 1500
CACCTCCCAG GCTCAAGCAA TCCTCCCGCC ACAGCCGCCC CACTCCCCAC CAGTAGCTGG 1560
GACTACAGAG CTGCACCACC ACACCCAGCT AATTTCTGTA GTTTTTTTTT TTAGTAGAGA 1620
CAGGGTTTCA CCACGTTGAC CACGCTGGTT TTAAACTCCT GAGCTCAATC AATCCACCTG 1680
CCTCGGCCTC CCAAAGTGCT GGAATTACAG GTGTGAGCCA CTGCACTCGG CTAGGAAACC 1740
CTTTTCTGAT CTTTCCTTGT CAGCAATGAT CTCTTCACAC TTCCTTTCTT ACGGCCCTCA 1800
CCTCACTCTG TATTATAGTT ATCTGCATAT ATGAATAAAA TCCCTAAGAA GACTGCAGGG 1860
TCCTGGAGGG AGGAGATCTG TATCGACAAC TTTGTCTCTT CTTCACAGCA CCTTACACCA 1920
GTGGGGATTT AAAAAGTGAA TACAGGGCTG GGCACCGTGG CTTATGCCTA TAATCCTAGC 1980
ACTTTAAGAG GATGAGGTGG GAGGATCACC TGTCGCCAGG AGTTCAAGAC CAGCCTGGCC 2040
CAACATGGCA AAACCCTGTC TCTACTAAAA ATACAAAAGT TCGCTGGGCG TAGTGATGCA 2100
TGTCTGTAAT CCCAGCTACT TGGGAGGCTG AGGCATGAGG ATTGCTTGAA CCCGGGAGGC 2160
AGAGGTTGCA GTGAGCCAAG GTTGCACCAC TGCACTCCAG CCTGGTTGAC CAGGTGACAA 2220
AGTGAGACCC TGTCTCAAAA AAACAAAACA AAAGTTTCCT GAGGGGAGTA GTATTTGAAT 2280
TGACAAGGTA GAGGGAGTGA AACGAAAGGT ATTCTAACCA GAAAAAAACT CAGACACCAG 2340
GAAAGAACAA ATAAGGGGCT ATGTGTAGGG TGGGGAGAAA GACAGCATCA GGTTTTCCAC 2400
TCGAGTCCTC TGTAGCTCTG CCTTAGCTCG CTGTTTAGTT TCCTTAAAGT ACCGACCAAA 2460
TTCACAACTA GTTTGTCTAT TTTCTTGCTA GTGCTTGCGA CACTAGAACA TAAGCCCGGT 2520
GAAAGGAAAA TAAATCTTGG GACCCCAAAA TCACTAAGCC AAAGAAAAGT CAAGCTGGGA 2580
ACTGCTTAGG GCAAACCTGC CCCCCATTCT ATTCCTTAAA AAGATAGCTA CTAAGATTTT 2640
TTTTTTTAAA AAAACTGCAT ACTGGGGCTG 2670