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

TagContent
EnhancerAtlas ID
HS098-27489 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr19:18587960-18590180 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11670056chr1918589943hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:18588029-18588048CGGCCACTAGGTGGAAGTC+6.74
HSF1MA0486.2chr19:18588554-18588567GAAGGTTCTAGAA-7.12
KLF4MA0039.3chr19:18588962-18588973CCACACCCTCT+6.02
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01013chr19:18588643-18590394Adrenal_Gland
SE_04099chr19:18587281-18588645Brain_Anterior_Caudate
SE_04099chr19:18588738-18590106Brain_Anterior_Caudate
SE_06012chr19:18587569-18592062Brain_Hippocampus_Middle
SE_09318chr19:18587289-18593113CD14
SE_12155chr19:18587989-18588691CD3
SE_12155chr19:18588799-18590417CD3
SE_15037chr19:18584199-18588821CD4_Memory_Primary_7pool
SE_15037chr19:18589123-18590617CD4_Memory_Primary_7pool
SE_17983chr19:18583928-18591813CD4p_CD25-_CD45ROp_Memory
SE_19379chr19:18587487-18590403CD4p_CD25-_Il17p_PMAstim_Th17
SE_20439chr19:18584612-18591598CD56
SE_21047chr19:18588603-18591663CD8_Memory_7pool
SE_22689chr19:18583973-18591671CD8_primiary
SE_23893chr19:18589312-18590189Colon_Crypt_2
SE_26168chr19:18588425-18592741Duodenum_Smooth_Muscle
SE_26932chr19:18588122-18592042Esophagus
SE_31681chr19:18586323-18588494Gastric
SE_31681chr19:18588601-18590332Gastric
SE_41123chr19:18587807-18590387Left_Ventricle
SE_41560chr19:18589244-18590155LNCaP
SE_42344chr19:18587292-18590373Lung
SE_44495chr19:18587274-18592340NHDF-Ad
SE_46271chr19:18587413-18593123Osteoblasts
SE_47511chr19:18588888-18589813Pancreas
SE_47511chr19:18589872-18590274Pancreas
SE_48120chr19:18587362-18592202Psoas_Muscle
SE_48694chr19:18588545-18590349Right_Atrium
SE_50125chr19:18585873-18593035Sigmoid_Colon
SE_51145chr19:18587336-18592595Skeletal_Muscle
SE_52434chr19:18585882-18592848Small_Intestine
SE_53541chr19:18587934-18592552Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr191858971418590055
chr191858920018589384
Number: 1             
IDChromosomeStartEnd
GH19I018472chr191858378718592442
Enhancer Sequence
AGACGTACGG GTATCGTGAG AGAGCCACGA GGGGCTTCTG GAGCTGAGAC ACGGAGGATC 60
GGAATGAAAC GGCCACTAGG TGGAAGTCAC AGCAGGCACC ACAGAAGAAA AGGGCAGCGA 120
ACTTGAAGAC AAAGCCACAG GAGCCACCTA GATGAATCCC ACAGTAAGAA GCCTACAGGA 180
AACGAACACC ACCTCGGTGA CCTGCGGACG ACAGCAGGGG ATCCCACGTG CAAGTAACTG 240
GAGTCCTGAG GGCAGGCGGG GGATCTGAGA AAAGAGTGGC CAGAGATTCC CAAATGTAAC 300
AAATGCTATA AATCCACAGA CCCAAGAAGC CTTGTCAACC CCCAGCAGGA AAACTACCAG 360
GTCGTGGCGC ATCATGAGCA AATCAGCACA GCCACAACAG TCGCCCCAAG TGCCGAGGTG 420
CCGACACTGC ACATCAGGAG CCAGCCCCGA CACTGGGAGG GCATCTTCAA AGTGCTGAGG 480
GAGAAACACC GCCAGACCAC AATTCCATGC CCAGTGAAAA GAGAAAGGGA AATAAAGATT 540
CGCTCAAACA AATGCTGAGA GAATCTTCTG TCAGCATCTG GCCTGCACTG TGAGGAAGGT 600
TCTAGAAGTT CTTCAGAAGG AGGGAGAGTG ACCCTAAATG GACCTATGGA TTTGCAGAGG 660
ATGACGCGGG CACAGTGAGC ATGCATGAAT AGAAAAGGCT TTTTTCTTAT GATGTTTCTG 720
CAAAAGATCA TTCAAGGCAT AAATTACGGT AGTGAGGCTG GGGTTTTGAA TGTGGGGTGC 780
TAAATAGATG GTGATGAGAA CACAAGGACT GGGTGGGGGG GATGAGAAAA AACACAGAAA 840
GCAGCTGGGG TGCAGTGCCC TGACAAGCCA ATCAAGGGCC CAGGAGGTGA GTGTCGGCTG 900
CAGACAGGCA GAGCCAGCTA GGTCCCTTCA CGGTGGGACC AGCTGTCACC CTCTGTGCTC 960
ACCAGCCTGG CCTGGTGGGG ACGCCTGACA GCATGTGGCC CACCACACCC TCTTCTGGCT 1020
GCTCCCTCCA GAGCCAACAT GCGTGGTGTC ATGGCCGAAC CCTTGTCAGG GGGGCCAAGC 1080
GCCTCGTTAC CTCATCTATG AAGCAGGACA GAGGGTCAGG AACAGACTGT AGCACAGGTG 1140
ATTTCCCTGC TGCCTTAGAA GCTTTGGGGT TGGCCTCAGG CTGCATTAAT TAAATAACGG 1200
GGTAACTCAG TAGCACATGA CACCTGCAGG GTACTGCCCA TCTCACACCC AAGAACACCC 1260
AGCAGGGGAG AGCCATGCCT CAGGCCACCG CCTGCCCAGT CTCTGTAGAC CCTCTGAGGG 1320
GTCATCACCC CCACAAGTCC TCTCAGGCCC TCGAGTGGCA AAAATCCAAC TTTCATTACC 1380
CAGCATGAGG TATGGAACTG GGAGCTCCTG AGATACAAAG TCACCCCCGC TGCTGTACTT 1440
CAGGCCAGGG CCCCAGGTGG GAGCTGGGGA GCCTGGTAGG GCCGCCACAG CTGGCCTGAC 1500
ACAGTCAGCA GGTCAGCTGG GTCTTCAAGG CCGGACAGGC AGGCACTGAG CTGTGCCGAG 1560
GCTGGTGCTC CCCAGACCCA ACTGGACTTC AGACCCTGAC TCGGAGAACA GACCTCAACA 1620
CAGCAGGGCA GTGATGCCTG CGCCCTGCGG TCACTTGGCC TGGGCGCCCA CTGGGGCTAC 1680
TGAACACAGA CTGGGAGACT CCTGTAGGCA GCTCCCCCTC AATGAGGACA CTCCTGTAAA 1740
GACAGCAATG CCTTTGGGAA AAGGGTCGAG GGTGCAGAGC CTGGGAGGCA GTGAGAGTCC 1800
TCAATGCTGA GACAGAGGAA AGGGTGAGGA GGAACCTCTC CAGGGCCAGA ATCCCCTGAT 1860
CCTCTCCCCT CCGGCAAAGA GCACTTCCGG GGATGAAGCA ACAGGAAGTG GCTTACGAAA 1920
TCCACCTCCA GGCCGAGTGA CCAGTTTACA GGAAGTGTGG TGGGTGAATC TTCCCCAGGG 1980
CACGAGGCAA TGTCTGGAGC CATTTCTGGT CCTCACCACT GAGGGCGGGG ACAGTCCCCA 2040
CCATCTGGCT CGGGGGAGGC CAGGGATGCT GCTCAGCACA CTGCAGGCAA CACAGAACCT 2100
CCTGCCCCAA ATGTCAAGCA GTGCAGGGGC TGAGAAGCCC TGGGCTGACC CTGCCACGGG 2160
AAGCGACCAT CAGAGCAGAA AGCAGAAAAA TCTATGGGAA AAAAGACCTG CTCCCTTCAA 2220