EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS029-07764 
Organism
Homo sapiens 
Tissue/cell
CUTLL1 
Coordinate
chr19:18616030-18619090 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4808136chr1918618867hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:18616238-18616256GGCAGGCAGGAAGGCAGG+6.77
HSF1MA0486.2chr19:18618282-18618295GAAAGTTCTGGAA-6.29
RARA(var.2)MA0730.1chr19:18618822-18618839AGGTCACATACAGGTCA+7.01
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_01013chr19:18616790-18618942Adrenal_Gland
SE_04099chr19:18612612-18621162Brain_Anterior_Caudate
SE_06012chr19:18609083-18619184Brain_Hippocampus_Middle
SE_08139chr19:18611825-18620707Brain_Inferior_Temporal_Lobe
SE_08861chr19:18618070-18618386Brain_Mid_Frontal_Lobe
SE_12155chr19:18614992-18619095CD3
SE_15037chr19:18615264-18618963CD4_Memory_Primary_7pool
SE_17983chr19:18613350-18619260CD4p_CD25-_CD45ROp_Memory
SE_19379chr19:18612797-18619131CD4p_CD25-_Il17p_PMAstim_Th17
SE_20439chr19:18615273-18618899CD56
SE_21047chr19:18616059-18618949CD8_Memory_7pool
SE_22689chr19:18615399-18619616CD8_primiary
SE_23216chr19:18612701-18620963Colon_Crypt_1
SE_23893chr19:18613414-18617350Colon_Crypt_2
SE_23893chr19:18617508-18618912Colon_Crypt_2
SE_26932chr19:18616253-18618743Esophagus
SE_30600chr19:18617865-18619920Fetal_Muscle
SE_31681chr19:18616275-18619182Gastric
SE_41123chr19:18609803-18620443Left_Ventricle
SE_41560chr19:18615472-18620976LNCaP
SE_42344chr19:18610919-18620435Lung
SE_46271chr19:18617926-18619177Osteoblasts
SE_47511chr19:18617763-18618281Pancreas
SE_48120chr19:18610995-18621599Psoas_Muscle
SE_48694chr19:18610987-18621062Right_Atrium
SE_50125chr19:18610975-18620517Sigmoid_Colon
SE_51145chr19:18609758-18621004Skeletal_Muscle
SE_52434chr19:18610979-18621003Small_Intestine
SE_53541chr19:18617401-18619093Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr191861637818616441
chr191861744918618539
chr191861840018618511
chr191861690718617225
Number: 1             
IDChromosomeStartEnd
GH19I018498chr191860923418621009
Enhancer Sequence
GTGTGCTTTC TTCTGCATCT GCCACAGCTC ACCCAACAGC AAATGCAATC CCAACTAGTT 60
AGGCTCTTGT TAGGACTGAA GATAGCTTTT GCTATTCTTC TCTACTCAAT TCTTCATCCT 120
AAGGATGCTG TGGCCAGTCA CACCCTCCCA CGGGCAAGGG CACCCGGCAA TAAGCCCCAG 180
CTACTGCCAT TACTCATCCC ACTTCCCAGG CAGGCAGGAA GGCAGGTGTG CAGAGCACTG 240
GGCAGGGCCA TAGTACCTGT GCCACACACA CACATGCTCT TCACCTCATC CAGAGTTTCC 300
TAGGTTTTGG TGCTTCAACA GCCCTCAGTA ACGCAGGCTC CTTACTATGA GATAGCCTGG 360
GAGAGAGCTG GGGTTTCTGT GATGGGAAAG GGCTAAGCCG GGAAAGGAAA CAGTGTGTGA 420
CTGGCGCCTT GCAAGCCACC TAAGGCACCA GGCACACACA GGGGAGGGGA GAAGAGGACG 480
GGAGAGGAGT GGGGGCCACG GGATGCGGCT TGTGTTCCCC TGATGTCCTG GGACACAGCT 540
CCCTGAACCC CAAAACACCC CACGGACAGG AAAGCAAAGT AAGGAGAGGT GAATGTGAGT 600
TGCAGGAGGG GCTGCAGGCA CTGACCTGAC CTCCCACCCA CAGGATGACC CCACACAGCA 660
GAGGGAGAAA CTGAGGCCCA GAGGGTGGCA CCACTGTACA GTCAGGTACC CCCACCCTGT 720
GTCCTGCTCT GTACTACACA GACCACCCAG CACACATGTG GCCAATACCA GTGAGGCAAA 780
GGTGGCAGCC TGGGCCCCCC ATGCTGGCCC TCAGCCATCC CTGGGACAAC AGTCTAGACA 840
CCCAGAAGCT CTGCACCTAG GCCCACTGAC CCAGCCTCCC TCCAAGCCCT GGGTGCCCAT 900
GTGTGCCCAG GCTGCTGCCC CTGGCACTCA GGCCATGCCA CACGCAGCAG CTGGGTCTGA 960
AGCCTGGCTT GGAACCAGCC CCCCACAGTC AACATGGAGA CAGCCCTGCT GGCACCGCCC 1020
CAGGCCTGGG CCCTGTCTCC CGCACCCTCC AGCGACCTGC CTGGGCCACC CTCAAGGTGC 1080
GCCTGCTCCT AAGCCGCCTC CCACAGTGGA GGGACACCCG GGCTGCTTCA GAGCAGACTG 1140
TGGCAAGTTA CCCTCTCCCC CAGGGGGAAA GGGATCCAAA GCTCCTGTGC CTCTGGGGTG 1200
CAGCATCAGC CCAGACTTCT GCTCGGCTGG GTGCCATGGC TCACGCCTGT AAGCCCAGCA 1260
CATTGGGAGG CCAAGGCAGG AAGTTCGTTT GAGGTCAGGG GTTTGAGACC AGGCTGAGCA 1320
ACACAGGGAG ACTCTGTCTC CATATAAATA AAAAATTAGC CAGGTGTGGT GCCACGCACT 1380
TGTAGTCCCA GCTATTTGGG AGGCTGAGGT AGGAGGATCA CTTGAGCCCG GGAGCCAAGG 1440
CTGCAGTGAG CTATGATCAC ACCACTGCAC CCCAGCCTGG ATGACAGAGC AAGACCTCGT 1500
CTGAAAAAAC AAAAGCAGAC TTCCGTTCAA CAGCATGTGA ACCTCACCTT GCACACCTAG 1560
GAGTTCGTTA CCCTCCTCAG CTCAGAGATT AGAGGGAACT CTCCCCACAG AGATGCTATG 1620
ATCAGAGGGC CAGGGACCCT GTCTCATTGA TCCTACGCTC TACGCCAGAC ATCGCCTCAG 1680
AATCCTTCTC AACACGGCTC CACTTCCTAT CTACAAGGAG CTGGCCTACA AGATGGAAGC 1740
GATTCCTACA TTATGGGGTC ATGTGGCTCC AGGCACATGG CCCTCGACCA GTGGGAGCCT 1800
GTGCACAGGT AAGAGAGCCA GGGCAGCCTG GAGATGAGCT GGACACAGGC TGCCAGCACT 1860
GGCTGTCCCC TCCCACTTGC CAAATCCAGT GTGAGCTGAG CACATTTCAC TGGAACAAGC 1920
AGGCGTCTGA GAGCATCCAA CTCCAAAAAT AGTGCCACCA GGAGAGGAAG GAACACGCTC 1980
TTCTAGCTGC ACCCGCTCCC TGCCCTCAGA TACCTCCCTG CACAGTCTGT GCCTGGCCTG 2040
TGGCAGTTCA AGGGTCACAC CCAACTCTGA AAAGGGAGAG ATAACATCCC CAGATAAGAA 2100
GAGTGAAAAC AGGCCAAGTC TGCTGCCAGA GCCTGGCCAC AGACCCACAG CCCCTTGGCA 2160
GAGAACTGCT CAGGAAGTCC TCCTCTGAGT CTTTCAAGCC ACTGGTATCT AACAAAGAAT 2220
CTAATCTGCA CACGGCACTT GCCCCGAGCT AAGAAAGTTC TGGAAGGGTC TCCTAGGTCT 2280
CCCCAGCCCA AGGTGAGCTT GCTTCTGTGG AGGGAGATGC CTGCCTGCCC ATGTCCACCA 2340
CCACTGCACA CCAAGCCAGT CTGAAGCCAC CATGATCTGG CTGTTGCTGG TTTATGGTGC 2400
ACCTCCCCGC TGCGAAGAAG TGGGCCATGT GAGCGCAGGG GCTTCATCCC TCCTGCTTCT 2460
TACTGGAGAA ACACTCCTGG AGGCAGCCGA ACCCTCACTG GGTGCAATCC CTCTGTGTAG 2520
GAGATTGCAC TGTGTAGGTT GTGCCCCGCC GAACAACCAC GCAGCTGAGG CTCAGCTCAG 2580
AGACTGCATT CAGAGCCCAA CTAGAATCAG ACACAGGTTC TGCGGGCCCC ACTACCCATC 2640
TGGAGGCAGA CGCCTGACCC CCAGCTCCAT CCCCAGAGAT GAGGATGCAG CAGGCTGAGG 2700
CTGACTCCAT GCGGCAGCTG CTCCCAACTC CACAAGGGAC ACACAAGCCA GCCCTTCCCA 2760
TCCAGGCTGC ACATGACTGT GTTTTGTTTC AAAGGTCACA TACAGGTCAC AAATAAAGAG 2820
GCCGGTTCCC ACTGGAGGCT ATGTCAGGAT TGATGCAGTC CCTGAGAAAA ACTCCCGGAA 2880
AACCCAGGGA CTCCCATGCG GGCTGAGAAA CATTTTGAGT TTGCATGAGA TCAAAATAGG 2940
AGTCACAGCT GAGTGTGGTG GCTCACGCCT ATAGCACTTT GGGAGGCCAA GGCGGGAGGA 3000
TCACTTGAGG CCAGGAGTTA ACAGACTGCA GTGAGCTATG ATCACACCAC TCCACTCCAG 3060