EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-14927 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr17:57924770-57926960 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11332131chr1757926392hg19
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: 40             
IDCoordinateTissue/cell
SE_00167chr17:57921765-57927189Adipose_Nuclei
SE_10048chr17:57913237-57927649CD14
SE_18111chr17:57922085-57925043CD4p_CD25-_CD45ROp_Memory
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_47932chr17:57925744-57925972Pancreas
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
CCATGCCCAG CCTTTTTTTT TTTTTTTTTT TTTTTTAATA CAGAACACAA ATTTGAGTGT 60
CATTCTTGTG CAGGGGCCAT GCTAATCTTC TGTATATTGT TCCAATTTTG GTGTATGTGC 120
TGCCAAAGCA AGCACCCAGC TTCTTTTCAT TAGTTAAGAA GATGAAGGCC AAGACTAAGG 180
CAGGGAGGCC TTTCTCTGCC TTTCACTCTT TAGTGCACCT CACAGTCAGT TGCACTTGAG 240
TAAGGACTGC TAAACCTCTC TGAGAGCTGC CAGATGTTCC TGCCTAGCCT CAGGTTGTTG 300
GTTCTTCAGA CACCTCTTCA TTCTGCCCAT TGCACCAGCC CTTTCCCATC TCCATGTTCC 360
CTCCATGGTA ATTTCTTTGT ACACAACAAC CACACGGAGC ACCAGCAATC AAGATTAGCT 420
CCCGGGAACT CTGGCGTGCC CTGTACCAGG AAGCACAGTG GATTACTACA ACTTTTGATA 480
ATGATTGTTT GCTTTGTACC AGGCATTATT TTCAGGGCTG TTTCACATGT GTTGTACTTA 540
ACAACCCCAT GAGGAAATTA AGGCAGGGTG GTTCAGTAAT TTGTCAAGGG AAACAAGGAA 600
GTAGAGCAGG CAGCAGAGGC GTTCTGGCTC TGAACTACTC TGTTCTGTAG AAATCAGTGC 660
AAAAGTCCAA GCTTCAGCAT ACTTGTTTCA TCTTGTGATC ACAGGTAGTT TTTTTTGTTT 720
TTTTTTTGTT GTTGTTGTTG TTGTTTATTT GTTTGTTTTG AGATGGAGTC TCGCTGTCGC 780
CCAGGCTGGA GTGCAGTGGG GCGATCTCCG CTCACTGCAG GCTCCGCCTC CCGGGTTCAA 840
GCCATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGGACTAC AGGCGCCCGC CACCTCGCCC 900
AGCTAATTTT TTGTATTTTT AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTC 960
AATCGCCTGA CCTCGTGATC CGCCCGCCTC GGCCTCCCAA AGTGCTGAGA TTACAGGTGT 1020
GAGCCACCGC GCCCGGCCCT GATCACAGGT AGTTGATGGA GAAAGGAAGA TAACAGAAAA 1080
TCAAGGCCAC AACCTCAAAT TTTGCTATTT AAATAGATAA GCAGACTTTA CTCTTCCCTG 1140
TATCACAGGG TTGGAAAAGC AAGCTCCATT CTTAGCCATC CATGTGGGCA GATTCCCAGA 1200
GTGGTGTTTG CTATAATTAT GATTTAAAAG CAAGGTTTTT TGTTTGTTTG TTTTAAGGAG 1260
ATGGGGTCTC CCATGTTACC CAGGCCGAAC TCCAACTCCT GGGCTCAAGT CATCCTCCCG 1320
CCTCAGCCTC CCGAGTAGCT GGGACTACAG GCACTCACCA CCACACTTGG GTAAAAGTAA 1380
TTTCTATTTC TACAGCCTTT TTTTATTTTT CAAAGTATTT TAATGTCTTG AGTTTGGGTT 1440
TTGTTTTGAG ACAGGGTTTC ACTCTGTTGC CCAAGCTGAA GTACAGTGGC GCAATCACAG 1500
CCACAGCTGA CTGCAACCTC CACCTCCCAG GCTCAAGCAA TCCTCCCGCC ACAGCCGCCC 1560
CACTCCCCAC CAGTAGCTGG GACTACAGAG CTGCACCACC ACACCCAGCT AATTTCTGTA 1620
GTTTTTTTTT TTAGTAGAGA CAGGGTTTCA CCACGTTGAC CACGCTGGTT TTAAACTCCT 1680
GAGCTCAATC AATCCACCTG CCTCGGCCTC CCAAAGTGCT GGAATTACAG GTGTGAGCCA 1740
CTGCACTCGG CTAGGAAACC CTTTTCTGAT CTTTCCTTGT CAGCAATGAT CTCTTCACAC 1800
TTCCTTTCTT ACGGCCCTCA CCTCACTCTG TATTATAGTT ATCTGCATAT ATGAATAAAA 1860
TCCCTAAGAA GACTGCAGGG TCCTGGAGGG AGGAGATCTG TATCGACAAC TTTGTCTCTT 1920
CTTCACAGCA CCTTACACCA GTGGGGATTT AAAAAGTGAA TACAGGGCTG GGCACCGTGG 1980
CTTATGCCTA TAATCCTAGC ACTTTAAGAG GATGAGGTGG GAGGATCACC TGTCGCCAGG 2040
AGTTCAAGAC CAGCCTGGCC CAACATGGCA AAACCCTGTC TCTACTAAAA ATACAAAAGT 2100
TCGCTGGGCG TAGTGATGCA TGTCTGTAAT CCCAGCTACT TGGGAGGCTG AGGCATGAGG 2160
ATTGCTTGAA CCCGGGAGGC AGAGGTTGCA 2190