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

TagContent
EnhancerAtlas ID
HS098-24651 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr17:57902230-57904570 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs115624974chr1757904302hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr17:57904512-57904533TGTCACTTTTTTTTTCTTTTT+6.17
RARA(var.2)MA0730.1chr17:57903777-57903794AGGTCAAGCGAAAGTCA+6.35
Tcf12MA0521.1chr17:57904264-57904275AACAGCTGCTG+6.32
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00167chr17:57902759-57904126Adipose_Nuclei
SE_02295chr17:57902600-57904669Astrocytes
SE_12351chr17:57902709-57903828CD3
SE_12872chr17:57903437-57909142CD34_Primary_RO01480
SE_13390chr17:57902679-57909156CD34_Primary_RO01536
SE_14102chr17:57902771-57904429CD34_Primary_RO01549
SE_14484chr17:57902818-57904522CD4_Memory_Primary_7pool
SE_18111chr17:57902713-57908324CD4p_CD25-_CD45ROp_Memory
SE_18274chr17:57902335-57909994CD4p_CD25-_Il17-_PMAstim_Th
SE_19224chr17:57902242-57909121CD4p_CD25-_Il17p_PMAstim_Th17
SE_25771chr17:57902310-57910881Duodenum_Smooth_Muscle
SE_27082chr17:57902825-57903450Esophagus
SE_28673chr17:57903913-57909888Fetal_Intestine_Large
SE_32541chr17:57902140-57911627GM12878
SE_33772chr17:57902955-57903499HCC1954
SE_33772chr17:57903886-57904476HCC1954
SE_34288chr17:57902535-57903657HCT-116
SE_34288chr17:57903725-57912037HCT-116
SE_34651chr17:57902404-57910911HeLa
SE_35896chr17:57902558-57903979HMEC
SE_37171chr17:57902077-57904585HSMMtube
SE_38933chr17:57902764-57904405IMR90
SE_44187chr17:57902422-57904694NHDF-Ad
SE_44824chr17:57902165-57904662NHLF
SE_45686chr17:57902159-57909893Osteoblasts
SE_47118chr17:57902074-57938709Panc1
SE_50387chr17:57904024-57904674Sigmoid_Colon
SE_51624chr17:57902428-57904733Skeletal_Muscle
SE_51976chr17:57902585-57903892Skeletal_Muscle_Myoblast
SE_52483chr17:57902778-57903765Small_Intestine
SE_52483chr17:57903903-57908944Small_Intestine
SE_54204chr17:57902041-57903813Spleen
SE_54204chr17:57903933-57904576Spleen
SE_55059chr17:57902384-57904733Stomach_Smooth_Muscle
SE_55921chr17:57902345-57909599u87
SE_59128chr17:57902596-57931450Ly3
SE_61214chr17:57902066-57937473HBL1
SE_62339chr17:57902123-57931675Tonsil
SE_63783chr17:57902538-57903970HSMM
SE_67474chr17:57902345-57909599u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr175790418657904344
chr175790281457903248
Enhancer Sequence
CTCAAAAAAA AAAAAAAAAA AAAAATTGGC TAGGCATGGT GGCTCACGCC TGTAATCCCA 60
GCACTTTGGG AGGCCGAGGC AGATGGATTG GTTGAATTCT CAGGAATTTG AGTCCAGCCT 120
GGTCTCGAAC ATGGCGAGAC CCAAAGTCAG GTGATAGAAC CAAAGAACTA GGGAACTTCT 180
AGCTCAAAAG GCATTATGTT AGTTGTGATT TTTTTTTTTT TTTTTTTTTT TTTTTGAGAC 240
AGAGTTTTGT TCTATTGCCC AGGCTGGAGC GCTGTGGTGC AATCTCGACC CACTGCAACC 300
TCTGCCTCCT GTGTTCAAGC GATTCTCCCG AGTAGCTGGG ATTACAGGCA CCTGCCACCA 360
TGCCTGGCTA ATTTTTGTGT CTTTAGTAGA GACAGGATTT CACGATGTTG GCTAGGCTGG 420
TCTCAAACTC CTGACCTCAT GATCCACCCG CCTTGGCATC CCAAAGTGCT GGGATTACAG 480
GCATAAGCCA CCGTGCCCAG CCCTTTTTGT TTTTTTAATT ACGATTTAAT ACTAATTTTT 540
ATTTAATTTT AGACTTTCTC CAGTGGGAGA GACCTGTGCA TATTTCTTAA AGAGCATAAC 600
CAAATCTAAC TTTTAAAGTT ATGATTAAAA TGACATGTTC CCATATTCTC ACCAAATAGG 660
GGATGTGAAT TCCCAGAAAA TAACATTAAG CATATGACTC GCAGCAAACC ATATGCAGAA 720
CATTGGCTCA TTGTCATGTT GCCAGGGTCT TATTGGAAGA CAAAGTCCCC AGTTTTACCA 780
CACAAGAAAA GTTTCCATAA CTCAATCATT GAACTTGAGG GCTGGGGGAT GGTGTTGGCT 840
GGAACAGGGA CTTTTTACCA GATACAGAAT GTTCCATGCT CTTCTTTGCT GTCTCCTATT 900
TCTGAGCTAA CTTGATGCTT GACCTCAGAG TCAGGCTTGC CTGTGGCAAG AGAGATCATT 960
TTAACCAGTG AGTAATAAAG TGCTTGAATC CGAATGTTGT TTCTTATCCC TCACTCTATG 1020
GAAAGTGGTC AGAATGAGCT ACGTGGGCCT GGACTTTTTC TTCTACAGAA AGAAAATCTG 1080
TCCTTTCATT TTAGAGGATA AAATGGTCCA TGTATTTGAT TCTCTTTGAC TTTGATCATT 1140
GAAAATAATC AGAAAAAGTT ATGGAAGTGT GGAACCCCAG CATTTGTATT ATCTGATGAA 1200
AGGATAGAAT TTAAGGCTTA ACACAGGGTT TAAACCCCAG CTGCCGAGAC TCAGTTATAC 1260
AGTCTAACAT AACCTCTTTC TGCAGCTTGG GAAAACCCCT TTCTCTTCTT GTCCGTGGTA 1320
GTTTATATAT CCTTCTCTTT TGACAGTTAA CCTTTCTATA TGTTTGTTAT GGATATTGGG 1380
AGACCACATA AAGGTTAAAA CAGGAGTTCT GGAGTTAGAC TGTTAGATGA GAAATGGGTA 1440
CATTGTATTT GGAAGTTACC GTTGACCATT TAATGGAGCA TTTTAGTAGC ATGATGAAAA 1500
TTAAAACCCA AATATATTGG ATTACATGGA ATTGTGGGCT AGAGGAAAGG TCAAGCGAAA 1560
GTCATGTCTG ACACATTTTA ATTGTTTTGT AAATATTTGT TGACCAGATG AATTAATTCA 1620
TTCATTAAAT AGGAGGGACC AGTGTGTATT TTAGGCTGAG GGAAAAACTC TAGTAAAATG 1680
CTAGAGATAG AAAATATAAA TGAAGAAAGG GAAGGATGTG GGAAGGAAAT TAACATTCAG 1740
TAAGCACCCA CTGTGCCAGA TGCTTTACAT AAATATTCAT TTCATATCCA TAACAAAACC 1800
TGTTAGGTAC TATTACAGAG AAGTTAAATT CATATAAATG ATAAGAGATG ATTGAGATAG 1860
GATCAATTCT GGAGTGGATT GATTATCCTC ATGAACCAGT TCTTTCTTGA AAACTGGAGT 1920
GAAGACTCCA AGATGTTTTG AGGCAGAGAA GGGGGACACT CCTGAGGGAG CACTCTGGAA 1980
GCCAGTGAAG TCATTTGCTG GAAGTTGGAA ATTTAGACTA GAGCACCAGT TTCAAACAGC 2040
TGCTGTGTGA ATTTGGTAGG GATGCAGCAT GAATTCTGTC TATTCTCCTG TGCACACGTG 2100
CATCCACCTG TGTGCAGCTG TAGCTAGTTA CTACTGTGGT TACTTTCAAT GAAAAACCTA 2160
CTGGTTTCTG TAGTGTACAT TTAAGTGCAT TTTTTCCCCT CTCCCAGCAT CCTTCTAGAT 2220
AGAGTTCCTT GAGGACAGAG ATCATAACTT TTTTTTAAGT GAGATTGAAT TTCAATCAAT 2280
ACTGTCACTT TTTTTTTCTT TTTTGAGACA GGGTCTCGCT GTGTTGCCCA GGCTGATCTT 2340