EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-12152 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr19:19598390-19601470 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:19601362-19601381CAGTGCCACCTAGAGGACG-6.49
FOXA1MA0148.4chr19:19599789-19599805TTTTGTTTACTTTAGA-6.69
FOXP2MA0593.1chr19:19599790-19599801TTTGTTTACTT-6.62
MITFMA0620.2chr19:19600216-19600234AAGGGTCATGTGACCAAG+6.19
MITFMA0620.2chr19:19600216-19600234AAGGGTCATGTGACCAAG-6.19
ZfxMA0146.2chr19:19601450-19601464GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_01191chr19:19597419-19601481Adrenal_Gland
SE_09215chr19:19595450-19601494CD14
SE_11973chr19:19597794-19601624CD3
SE_13867chr19:19597292-19601474CD34_Primary_RO01536
SE_14578chr19:19595555-19601818CD4_Memory_Primary_7pool
SE_17284chr19:19597785-19601599CD4p_CD225int_CD127p_Tmem
SE_17695chr19:19595455-19601775CD4p_CD25-_CD45RAp_Naive
SE_18023chr19:19597051-19602095CD4p_CD25-_CD45ROp_Memory
SE_18475chr19:19595670-19601884CD4p_CD25-_Il17-_PMAstim_Th
SE_19438chr19:19597486-19598710CD4p_CD25-_Il17p_PMAstim_Th17
SE_19438chr19:19598715-19601649CD4p_CD25-_Il17p_PMAstim_Th17
SE_20088chr19:19597646-19601744CD56
SE_22348chr19:19595603-19601745CD8_primiary
SE_24291chr19:19597429-19601354Colon_Crypt_2
SE_29832chr19:19598800-19601612Fetal_Muscle
SE_31176chr19:19598232-19601563Fetal_Thymus
SE_32371chr19:19598258-19599891Gastric
SE_32371chr19:19599909-19601478Gastric
SE_37262chr19:19598596-19601447HSMMtube
SE_41770chr19:19596688-19599943LNCaP
SE_41770chr19:19599953-19601445LNCaP
SE_42846chr19:19598281-19601556Lung
SE_50636chr19:19598249-19601453Sigmoid_Colon
SE_53638chr19:19595818-19601579Spleen
SE_55298chr19:19598271-19601370Thymus
SE_69075chr19:19598313-19601571H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr191959884919601381
chr191960001219600395
Number: 1             
IDChromosomeStartEnd
GH19I019484chr191959561619601954
Enhancer Sequence
TGCTCAGACC TGCACTCCCC CGAGTGGAAC CCCGAGTTCT GCCATGACCT TCACCCCGAG 60
GCAAGGGGAC AGGGCCGGGC AGGCTTCCTG AGGCATGTTG AAGAGGGATG TTCTGCAGGC 120
AGAACATGGC CATGCTGGGC CATGTCTGTG GGCCAGGCCC CAGGAGGGCG GGGGATGTTA 180
ACAGCTTGGT TCATGTCAGG TAGGGCCTGG TGAGCCCAAG ATGAGTGTTT GCACAAGGGA 240
CAAGTGAGCT GGCAGGGCTG GTGTTGGCTC TAGCAGAGCC CTCATCCCAC CCTTGCACAC 300
AGCCAGCAGC CCACCCTGCT AGGCCTGAAA GAGGTGAGGA GGAAAGGTTC TAGTGGGAAA 360
TGGTTCTGTG GCTGGAGAAG GCATTGCTGG GCCCTGCCTG TCTCCCCAAG CCAGCCTGGA 420
GGAGGATTTC TTGTACCGAG GCCTCACGAG CTACAGGTCA TGGTCATCCC TAACTTCCCT 480
AGTGTGTGCA AGACTTGGGG GATCTTGCTG AAATACAGAC TTTGATCAAG CAGGTCTGGG 540
GCAAGGAGGA CACGCTTCAT TTATACAAGT TCCGGAGAAG CTGCCCTGCT GCTATGGCGG 600
TGACAGCGGT GGTCAGACAT TCACGGGGCC AGCCCCAAGC CCACCTACAG CCTTGCCCCC 660
ACCTGCCGCT CCCCTGTTGT GTCTGTCCAT CCTGGTAGAC TGAACCCTAA GGACAGAAAT 720
TCCTTTTATC CAGGGGTTCC TCCCCACTGC CTGCTATAGC ACCTGCTTTT TAAATGAGCT 780
CTCAGCAGAT GTAAGGAATG AATGAATGAA TGAATGAGGG AGAGGGGTAT GTCTTTCCTG 840
CATACCAGGC AGGCCTGTTC AGAGAACCAC AAAGGTCCCA GCCTCCAAGG ACAGCTCCTT 900
CCCGGCACTG GCTGAGGGGA CACTAAATAT TAACCACGTA CTGGCCGCTG GTTGCTGAGC 960
AGCTGAAAGC CATAACCTTT TGCTGTGGAA GTGGGATCGT GTCTCAATTT AAGTTTATAA 1020
TCCCGGCCTC TCCTCCAGGA AATTCTATGG AAGTTCCTGG CAGGTAACAG AATTTCTGTG 1080
CTTGTGAGGT CAGGGCCAGT GCCAGCGGGT CAGGGAGTGG GGGTGGTGCG TGTCAGCGAG 1140
CGGGTGAGAC CATTTACGCT GATAACAGCC TGGCCTGCTT CCAGGGATTT TTGTAGGTCA 1200
CATAAAATCT CTTGATCACT ACGTTTTACA TTAAGGCTTC TCAAGATGGG CAGGACGGGC 1260
TTATGGGATT TGTCCTGAAC TATCACATCA CTTCCAAATA AACTTGGTGC CCGGGACGGC 1320
TGCTGTGGAG TGAATGGCAG ACGCTGTCCC TGGGCCACGA TGCCATCCCT CTCAGCATGT 1380
TGGGCTAGAT TTCCACTGGT TTTGTTTACT TTAGACAGTT TTTATAATTA AATATTTCCC 1440
TGAAATAATG CCTGCAATCA TTTTGAGCCA CATGCTCTTT TTCCTGAATT AAAGATCTCT 1500
TTTAGAAAGT ACTGAGACTC TTAAAGCCTC TCTCCTTTAA AAAGTGAGCT TAACAAAGTT 1560
TTTCATTTTA GAAACTTAGA GGGGCCAGTG ACCCTGCTGT GTGCGGTGTA TGTAGAGGTG 1620
ACTGGAGCCT GTGGTGCAGC AACAGTCCCC TGTGGGCTGG CGCCACACAG GAAGTGCCTG 1680
CAGCTCCACA GCCCTGGGGT GAGCCTGGCG CCTCCATTTT CTGACAGTAC CTGAACCTTT 1740
ACCTCCCTTC TCAAAATGAA GGCTGCGTGT CACAAACCGG TTGGAACTGG CCGTTGCCAT 1800
GGTTTTCACG TTGGAAGGCA CAGTTAAAGG GTCATGTGAC CAAGGAGGGA AATGCCTTTG 1860
TCACATGACT TTTTGGTGGC CTGATTAGCA TACAGGAAGT TCACTCCCTG CTGGCTGCTG 1920
GGATGCTGAG TGATCATTGA TGGGTGGTGA CATCATCTCT TGGATGAGTT ATTGATTAGT 1980
CGCAGGCCAA GATGGGGCCA GGGAGCGCTG TGGGCAGAGC AGCCCTCTCA GGCAGCTTCA 2040
GCTGCTAGGT GGTCTGGACC CCTCGCCTAC CCTCTTCCTT CAGGCAGGTT TGAATTTTAT 2100
TAGACATCTC ACCTCTGGAA GAAGCACACG CCCTCAATAA GATGATAAGA AGGGTTAAGT 2160
CCCTTAGAGC TTGGCTGTCA TTTCATTTCA GCTCATGCTA GCCCAGGAAT TGTGTCTGTA 2220
ACTCTATACA AGATGCTGCC TTGGCCCCCT GCTCCCCTGT TCACTTTGGA GGCCACCTGG 2280
GTGGAGGCCA GCTGCTGCAC CTCTGTGCTG AAGCCTTGGG ACTGCCTGCC TCTGAGGTGC 2340
TCAGTGTGTG TACACGTCCA GGGAACCTGG AATTAGAGCC CTGAGGTCAC CTTGAAAGTC 2400
GATCTTGGGC GGCATGGGGC CGGCAGCAAG GAGAGACATG CTGGCGGTTT GCTAAGACCT 2460
GAGTGAGGTG TCCTGGGTTA CTTTAGAAAC AAACTACCCG GTTCTGGGCT TCAGAATGTG 2520
GGCTGATAAC CCCTTGCCTG GGGGATTGTA TACTTCGAAA TCGTACCTTT CTGTCCACGC 2580
CCAGGTCTCT GGTGAGAAGC TGCTTCATCA GGGCTAGGAC CAGCGTTCAG GTACAGCCAC 2640
CACGTAGCTG TGGTGGGTGG AATTAGGAGG GACCAGAGGA GAGCAAGTAA AGCGGTTCCT 2700
GAGTCCAGCA TCTGGCGAGT CCAGGGTAGC ATTGGTGAAG CCTTAACCTC TGGTGCTCTG 2760
TGTCTACCCT TCCCTGAGGA CGCAGCTCAT GGGTGTGGAG GGGACCTCAG AGGTCCCGAG 2820
GGCTGCTAGA GCAGAGTCAG GTTCTTCATC CTAGCGACTC TCCTCAACCC TGCCGGGGTC 2880
TAATTATCAA CTAGACCCTG GCACAGCAAG AGCCAGGACA ACTTTGAGCT GCGGCAACCA 2940
GTTAACTTTG TCCGAGTTTG TTCTCTGGGT CACAGTGCCA CCTAGAGGAC GTGTCTGTCC 3000
TTGGCTGGTT TTCCTGCTGA CAAAAAAAAT GGACTTGATT CACTTCGATG AATGTACAAT 3060
GAGGCCGAGG CGGGCGGATC 3080