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

TagContent
EnhancerAtlas ID
HS012-16035 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr2:43419880-43422730 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12614953chr243421461hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr2:43421880-43421891TCTTATCTCCC+6.62
PAX6MA0069.1chr2:43421205-43421219CCCTCATGCGTGAA-6.06
RARAMA0729.1chr2:43420740-43420758CACTGACCTGCTGACCTT-6.26
TCF7L2MA0523.1chr2:43422153-43422167GTCCTTTGAAGTTT-6.1
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_03102chr2:43421033-43422155Bladder
SE_11879chr2:43418911-43423261CD3
SE_13409chr2:43420281-43422935CD34_Primary_RO01536
SE_14384chr2:43419736-43423391CD4_Memory_Primary_7pool
SE_16107chr2:43418889-43423186CD4_Naive_Primary_7pool
SE_16950chr2:43419718-43423194CD4p_CD225int_CD127p_Tmem
SE_17323chr2:43418298-43424856CD4p_CD25-_CD45RAp_Naive
SE_17875chr2:43418720-43423486CD4p_CD25-_CD45ROp_Memory
SE_18565chr2:43418586-43425101CD4p_CD25-_Il17-_PMAstim_Th
SE_19552chr2:43419045-43424825CD4p_CD25-_Il17p_PMAstim_Th17
SE_20901chr2:43419730-43423348CD8_Memory_7pool
SE_22349chr2:43418758-43425198CD8_primiary
SE_23059chr2:43418495-43422765Colon_Crypt_1
SE_23724chr2:43419841-43422740Colon_Crypt_2
SE_24685chr2:43419715-43422905Colon_Crypt_3
SE_25333chr2:43419730-43423364DND41
SE_26374chr2:43419705-43422902Duodenum_Smooth_Muscle
SE_26557chr2:43421228-43422781Esophagus
SE_27617chr2:43418343-43423099Fetal_Intestine
SE_28536chr2:43418392-43423198Fetal_Intestine_Large
SE_30898chr2:43419713-43423304Fetal_Thymus
SE_31392chr2:43419752-43422761Gastric
SE_34919chr2:43422110-43423362HeLa
SE_40066chr2:43420058-43423419K562
SE_42201chr2:43419809-43422274Lung
SE_49954chr2:43419904-43422270RPMI-8402
SE_49954chr2:43422272-43422938RPMI-8402
SE_50052chr2:43418452-43423001Sigmoid_Colon
SE_52337chr2:43418468-43423283Small_Intestine
SE_53288chr2:43420099-43422793Spleen
SE_58412chr2:43352450-43425007Ly1
SE_61450chr2:43354337-43468354Toledo
SE_62203chr2:43354169-43468733Tonsil
SE_65350chr2:43419451-43422721Pancreatic_islets
SE_66787chr2:43420870-43422147Jurkat
SE_66787chr2:43422197-43422944Jurkat
SE_68698chr2:43421113-43422308H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr24342122943421631
chr24342200543422472
Number: 1             
IDChromosomeStartEnd
GH02I043190chr24341729043424879
Enhancer Sequence
AAAAAAAGTC ACTGCTTGGC TTCTTTTTGG TTCTGGCAGG CTGGGCCCAG CCCAAGTGTG 60
GCATGTGAGT GAACCACCCA GAGGAGGGCT GGGGGCTTGG CTCCTGGGGG CTCCAGTAGC 120
TCCCTGCGAC CTATCTCTGC CCCTCAAATC CTTCCATTCT AAAGGCCAGC TCCATGCCCA 180
CCTCCTCCAA GAAGCGCCAG CTGCTGCCCC CAGGCCAGCC TCCACCTGCT CCCACAGGCT 240
GGGGAGTGGT CAGGGAGGGT TTGCAATGTC CAGCTGCCCT GTCTCCTGTC CCAGGCAGCG 300
ATGTGTCCAG GGCTCCATAC CAGCTCCAAG CTCTCTGCCT ACAGCTCCCT CACATCCACA 360
CTCACTGGGT CCCAGCTGGA GACCTGGTGG CTTTGAGAGG ATACCGTGGC TTCTTGATGT 420
ACCTGAAGAC TTTGGAACGC CAGAAGTGTT CAGTCCTGTG ATGGGTGTCA GCCAGGCCCA 480
GAAAGCACAC AAACTGGGGG ACACATATGC TAAGTTATCC AGAAAGCCTC AGGGCTGGGG 540
CTGGAAGAGG AGGGCCTTGC CATCCCAAGG TGCTGGTGTG TCCACACGCC CCTGGGGTGA 600
CCGTGTGCAT CTGTGTGTGT GTGTTTGTGG GTGGGTGGCT GACTACTCTG AGTTTGTGGG 660
TGATTCATGT GTACCCTCGC GACAGGCTGT GTTCAGATAG TCTGCTTATG TGCTTGAATT 720
CAAGGACACA AACATCCCTA GGTGCAAGCT TGCACGCACA GTCCTCCCTA CACCTCCACA 780
CGCAACTCCT AATCATCCCT CAGGATCCTC TCCCCGCCCT GCTTCAGCCT TAAGGCCTGC 840
TCTGACCCTC CAGCCCATCC CACTGACCTG CTGACCTTCA TCCCAGACAC TGCTGGGTTC 900
AGCCCTGGAG CCTGGTCACT CTTGCTCCCT GAGGGTGAGG TTGACTCCTT TTTAAATTAC 960
CCCTAAAGCC CCACTTAGGG AGACACAGCC TTATCAATCA ACACTCCTTG AATGAATTAA 1020
AACAAACTCC AAGGAAAGGA ACTGCATTTG GGTGGATGGA AACAAGAGCT CTCAAGCTGT 1080
TTTCTTTCCT CTTTACCCTT TGCTCTCTGT CTCTTCCCAT CTGTACTTTC TCTAACTTGT 1140
TTGCTAACTC AATCGTCAGC TTAGAAAGTA CTTCCTTGTA TACCCTCCTC TCATTCAAAT 1200
CTCATGACAA TCCTCCAAGA CACGAATAAT TATCCTCATT GCACAGATGA GGAAACTGAG 1260
GTTCAGGGAG GCTACGTGAG TTGCCCAAGG TCACACAGCC TGGAAGGAGT GGGTAGGGAC 1320
TAGAACCCTC ATGCGTGAAT GGACACCACC TCCCACCACT CCCCACCAGT AAGTAGAGGG 1380
TGGAGGGTAA AGGGCGATCC AGGGGCTCGG AGAGGATTGG CCTCTTCAAG CCCTCTCCAT 1440
GGCCCAAGGT CACCGTGGGA GGGAGATGCA CCTGGCCCCC AGGGCCAGGG GTTACCCCAC 1500
TCGGCCAGCA ATGGGAGAGG CCATGAGATC TGTGGACATT GTTCCTGGGC CTGTGGTTAC 1560
TGATTTGACA ACAGCCCTGT TCCTCCCCAG CCAGCCAGGG AGTTAATGAT TAAGGAGGAG 1620
ATTAAATATT AACCACCTGT GGGGCCACGG CGTAATGTCT CCATCTGCAC CTGAGCCTAC 1680
CTAAAAATCC CTCCCACCTG CCGTGGGCCA GCCCCACACA GGGCCTCTAA GCCCCTTGCT 1740
TAGGGATACC ACTTCCCCAT GCCCCCATCC TGCCCTGGCC CTGGCCCTGG CCCGTGTCCA 1800
CCCCATCTCA CTCTCTCATA CCCACAGCAC AGACCCAAGG ACTCTTCCTG TAGCTTGGAA 1860
GCTGCAAGCT ACACCACTGT AGGCACTCCT GGTGGGCCTT CTGGAGGAGA GGACCTGCCT 1920
GAACCCAGCT ACTCCTGGGG CTTGGAGAGT CCGCAGGTTA CATTCCTACC TGTGACCTCG 1980
TTTATCAGTG CTCTTATCGC TCTTATCTCC CAAGTCGTTC CTCCTAAAGA CCCCTCTGAA 2040
TCTACACATC CCAGGCCCCA ACACCCTGGG CTACAGCAAC TCCCCAACAC GCCATTCTCT 2100
TCTTTCTTCT AGCAGTTAGA ATCTGGGTGT GTTCTGCCTC CAGGAAGCCT CTCATATTAA 2160
CCTGGGCTAA GGTCTCTGCG GGCCTCTGCT CCCCAGCTTC CCTTAGGCCG GGGTGATTCA 2220
GGCTGGCATT GGCTGCTGCA CGGCTGCAGG AAACCAGCTG CATCTGTTGG AAGGTCCTTT 2280
GAAGTTTAAG TGCACAGCCT CCGAGCGCTG GGGGCGGGGA CTGCTCTATC TCACCTAAGC 2340
CTAGGGCCTG CCCCTGGGTG AAGCCATGGT CACCCTCCCC ACAGCAGGAA CCACAGGCAG 2400
TATGACACAG GGTTCACCTG CGTCTTTTTC TATAAATATA GAAAAATGGA ATTATTTATT 2460
CAAATAATAA CTCTATTGAT ATGCTCTCAT TCCTGTTTGT GGGGAAGCCC CAGATGACTG 2520
TGTGGGTAAG TTACTATGGT ACGTAAGCCC CACCGTAGCC TGGGCCTGCA CTGCTCTCTC 2580
TGCATGTCAG TGAACTGCAT TGACACTGCA GGCCTAGTGA CAGGCAATGT CATCCCCATT 2640
TTACAGATGG CGAAACTGAG GCTGGGTGAA ATTAAAGGAC TTGGCCACGC TCAAACAGAC 2700
AGGAAATGGC AGAAGCTGGC CTGCCTGGTG CAAAAGCCAT ACAAAACTGA AAAGGACCTA 2760
ACACCGTTCT TGCCACAGCT GTCTAGGCCC CAAGCTCAGC TTCTTTTCAG CCACAGTTCC 2820
CAACCATGTG TGGCTTGCTT GCTTTTCTTT 2850