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

TagContent
EnhancerAtlas ID
HS127-11077 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr15:81589420-81591720 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4778636chr1581591639hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MecomMA0029.1chr15:81589472-81589486GGGATAAGATAAGA+6.12
NR2F1MA0017.2chr15:81591262-81591275CTCATGACCTTTG-6.3
RESTMA0138.2chr15:81589589-81589610GGTGCTGTCCAGGGTGGGGAG-6.5
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_09274chr15:81584718-81607275CD14
SE_10222chr15:81583256-81598058CD19_Primary
SE_10932chr15:81575890-81613656CD20
SE_12059chr15:81583291-81590601CD3
SE_14915chr15:81583300-81599266CD4_Memory_Primary_7pool
SE_15536chr15:81583334-81593848CD4_Memory_Primary_8pool
SE_15975chr15:81582456-81593036CD4_Naive_Primary_7pool
SE_16447chr15:81583829-81596703CD4_Naive_Primary_8pool
SE_17122chr15:81583421-81593670CD4p_CD225int_CD127p_Tmem
SE_17378chr15:81576404-81611753CD4p_CD25-_CD45RAp_Naive
SE_17965chr15:81582772-81600449CD4p_CD25-_CD45ROp_Memory
SE_18364chr15:81581577-81610103CD4p_CD25-_Il17-_PMAstim_Th
SE_19384chr15:81583544-81599119CD4p_CD25-_Il17p_PMAstim_Th17
SE_20326chr15:81583075-81599877CD56
SE_21334chr15:81587876-81593826CD8_Memory_7pool
SE_21613chr15:81583315-81595262CD8_Naive_7pool
SE_21977chr15:81583297-81599385CD8_Naive_8pool
SE_22527chr15:81582319-81600599CD8_primiary
SE_31057chr15:81583528-81595709Fetal_Thymus
SE_43620chr15:81584897-81596053MM1S
SE_50253chr15:81583295-81597455Sigmoid_Colon
SE_53136chr15:81583768-81597247Small_Intestine
SE_53661chr15:81583770-81597299Spleen
SE_55142chr15:81583759-81592012Thymus
SE_58690chr15:81576351-81605600Ly1
SE_58859chr15:81583158-81611021Ly3
SE_61873chr15:81576243-81605254Toledo
SE_62258chr15:81567470-81610802Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr158159018581590430
Enhancer Sequence
TAAGCTTTCA TTGAGATCTT CCAAAAGGAA GGGTCTTTTG AAAAAAGGTG CAGGGATAAG 60
ATAAGAGCAC AAATTGGCCT GAGGATCAGA GTGCTCTGCA TTGACATCAC CACTGGACCT 120
GGCTGATCAA CAGTCAAGGG TTCCAGGTGC TGGGCAGCAG CACCGTGGAG GTGCTGTCCA 180
GGGTGGGGAG CCTCCTGGGT GGACGGGTGA TGCTGTGGGG GTGGCAGCAG GAATGCAGGC 240
CATTCTGGAT AATTGGGAGG ATGGAGCCCT TGGAAGAGGT CCAAAGACAC ACCCACCCAG 300
CCATCCTGGG CAGCTACCTC TAGGGTGCCA ACATTCCAGT TGCAACAGTC CTGCTGCATT 360
CAGGATTTCT GAGTCAGAGA ATGCAACGCC AGAAAAGTAT AAATAGCATC TACCAGTGGT 420
CACCTCCTCC ATGAGGTGGA TAGCAAGGGT GTGTCCACAT GGTACACCTG ACAATGCTAA 480
GACATGACTT GAATATTTAT TTGCTTGCTA GAGAGAGCAT AGGACTTGAA GTCAGGGAAT 540
CCTGGATCTG TCTGTCATTA GTATGATTCT GAGCAACCTA CTTTGCCTTT CTGAGCCCAG 600
ATTCACTCAT CAGCAATGTG TGGAAGAGCA CGTAGACCCC AAGCATATGA TGCATTCAGC 660
AAGCACACAT TGAATGCTGG CTTCGTGAGG CCCTGTGCTA GATGCTGGGG GGAGAGAGAG 720
AAAGGGATGA GACCAGGTAG TCAGGTCCTG CCTCCAAGGA GCAACTAGTA GTGGCAGGAA 780
ATAAACATAT AGACTATAAA ACATATGACT GTTTGAGTAA CACTACAGAA AAGCTCATGA 840
AAGACTTTTG GAGGGCTAAG GGACATTTTG GAAAGATCTA GCACATCTCA CCCAGAGCAG 900
AGGCCCTGTG GGTGGAGGCT CCTCTCCCTT AGTCACCCTA ATTGAGGAAC ATTCTAGCAA 960
AAGCAAACGC CTCAGTGTTT AACTGACAGG AGGTTGTCAC TCCAATCTGC AAAGGGCTTG 1020
CCTGTGGAAC CTCTGCCTCC TGATTCTCAC AACAGCACCT TACAGCCAAG CCATTCAAAA 1080
ATGCAGAAAC AGGCTGGAGG CCTGGGCTCA CTTGCCCAAG GCCAGTCTCT TAGATTGTGC 1140
AGAATTTCTC TTTGATATCA TCAAGGTGTA ATGCTCCATG ATTCACTTCT TTTGAAACCT 1200
GGCATTGAGA CAAGGGACAG GAGGGATCAG AGTTCCTTCA ACTGGGTTGC GTTCCAGTAG 1260
CAAGCATCCC CCAAGGCACA CAGGCCAGCC TCCCTCTGCC CCTGGGAAAG AGAGCCAGGA 1320
CACCCTCTCC CTTACCCATG CAGATATGAT GCTGGTTCAA TGCTGGCTTC TGAGAAAGAC 1380
TCCTATGTGC TCCAGGGCAT GCCTGAGGTC CTGGCTGGCA CAGAGCAGGT TGCACATTGC 1440
AATCCCCTGC TCATCACATT CCCAACACCC AGGCTGCATC CCAGGTATCT TCAGTCAGTA 1500
CCTAGGGGTG GGCGTCAGTA TTTTTCAGGG CCCTCCAGAT TCCAGTATGT AGCCAAGGTG 1560
GAGAATCCTA CTTCACAGAT TCCTTTCTAC CTGGAACCTT TTCATCAGCT TTTGAGGGAG 1620
GGAAAACACT CCTTTGCCGA GAGCAAGCTG ATCAATGACC TGTGTATAGG CAGAGCAGCA 1680
AACACACGGC TTCAGGGCCA GGCAGGTACA TACATGGGAA ATGCTGGCTG GGTGAGAGGG 1740
AGCGTGAAGA GCTGTGGGAA GCCGAAGTGG CCCCATCAGA AGCTGTGCAC AGGCACCTTG 1800
TTTTTAATGA CACGGGTAGG TCAAAGCACA AACAGCTGCC AACTCATGAC CTTTGTCTTA 1860
AAAGTTTAAA CGGCAGGAGA ACTGCTTTGG CTTTTACACA TTTAACATGG TATCTTGGAG 1920
GCTCCTTAGT GCAGTAGAAA GGACATGAAC TTCAAGAGTC AGGAGACACA GGGTCTTGCC 1980
TGAGCACTGC CATCAGATGG CCCCTTACCC TTCTTGAAAT GTAATATGCC AGAGGTCGGC 2040
CCAGATATTC TCTGAGCACC CTTCCAGGCC TAAAACACTA GGATACTGTG AGATTAACTC 2100
CTACTTCTGG TCCTTCACTC CTGCCTGTTG GCAGCTCAGT CAGGTAATAG CACCTGGAGT 2160
TCACCCACCT GGGTGTCCCC CACTTCTGCT AATCTCCTCC TCTTGAATCC TTCTTGCTGT 2220
TCAGCTTGGA AACTAGAATT TAGGAAGAAA AGTCACTGTA TGATGTAATG CACAGCTTTG 2280
GCCTTGTTTC TGCACTGTAG 2300