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

TagContent
EnhancerAtlas ID
HS044-07034 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr2:43419900-43422680 
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
TTCTTTTTGG TTCTGGCAGG CTGGGCCCAG CCCAAGTGTG GCATGTGAGT GAACCACCCA 60
GAGGAGGGCT GGGGGCTTGG CTCCTGGGGG CTCCAGTAGC TCCCTGCGAC CTATCTCTGC 120
CCCTCAAATC CTTCCATTCT AAAGGCCAGC TCCATGCCCA CCTCCTCCAA GAAGCGCCAG 180
CTGCTGCCCC CAGGCCAGCC TCCACCTGCT CCCACAGGCT GGGGAGTGGT CAGGGAGGGT 240
TTGCAATGTC CAGCTGCCCT GTCTCCTGTC CCAGGCAGCG ATGTGTCCAG GGCTCCATAC 300
CAGCTCCAAG CTCTCTGCCT ACAGCTCCCT CACATCCACA CTCACTGGGT CCCAGCTGGA 360
GACCTGGTGG CTTTGAGAGG ATACCGTGGC TTCTTGATGT ACCTGAAGAC TTTGGAACGC 420
CAGAAGTGTT CAGTCCTGTG ATGGGTGTCA GCCAGGCCCA GAAAGCACAC AAACTGGGGG 480
ACACATATGC TAAGTTATCC AGAAAGCCTC AGGGCTGGGG CTGGAAGAGG AGGGCCTTGC 540
CATCCCAAGG TGCTGGTGTG TCCACACGCC CCTGGGGTGA CCGTGTGCAT CTGTGTGTGT 600
GTGTTTGTGG GTGGGTGGCT GACTACTCTG AGTTTGTGGG TGATTCATGT GTACCCTCGC 660
GACAGGCTGT GTTCAGATAG TCTGCTTATG TGCTTGAATT CAAGGACACA AACATCCCTA 720
GGTGCAAGCT TGCACGCACA GTCCTCCCTA CACCTCCACA CGCAACTCCT AATCATCCCT 780
CAGGATCCTC TCCCCGCCCT GCTTCAGCCT TAAGGCCTGC TCTGACCCTC CAGCCCATCC 840
CACTGACCTG CTGACCTTCA TCCCAGACAC TGCTGGGTTC AGCCCTGGAG CCTGGTCACT 900
CTTGCTCCCT GAGGGTGAGG TTGACTCCTT TTTAAATTAC CCCTAAAGCC CCACTTAGGG 960
AGACACAGCC TTATCAATCA ACACTCCTTG AATGAATTAA AACAAACTCC AAGGAAAGGA 1020
ACTGCATTTG GGTGGATGGA AACAAGAGCT CTCAAGCTGT TTTCTTTCCT CTTTACCCTT 1080
TGCTCTCTGT CTCTTCCCAT CTGTACTTTC TCTAACTTGT TTGCTAACTC AATCGTCAGC 1140
TTAGAAAGTA CTTCCTTGTA TACCCTCCTC TCATTCAAAT CTCATGACAA TCCTCCAAGA 1200
CACGAATAAT TATCCTCATT GCACAGATGA GGAAACTGAG GTTCAGGGAG GCTACGTGAG 1260
TTGCCCAAGG TCACACAGCC TGGAAGGAGT GGGTAGGGAC TAGAACCCTC ATGCGTGAAT 1320
GGACACCACC TCCCACCACT CCCCACCAGT AAGTAGAGGG TGGAGGGTAA AGGGCGATCC 1380
AGGGGCTCGG AGAGGATTGG CCTCTTCAAG CCCTCTCCAT GGCCCAAGGT CACCGTGGGA 1440
GGGAGATGCA CCTGGCCCCC AGGGCCAGGG GTTACCCCAC TCGGCCAGCA ATGGGAGAGG 1500
CCATGAGATC TGTGGACATT GTTCCTGGGC CTGTGGTTAC TGATTTGACA ACAGCCCTGT 1560
TCCTCCCCAG CCAGCCAGGG AGTTAATGAT TAAGGAGGAG ATTAAATATT AACCACCTGT 1620
GGGGCCACGG CGTAATGTCT CCATCTGCAC CTGAGCCTAC CTAAAAATCC CTCCCACCTG 1680
CCGTGGGCCA GCCCCACACA GGGCCTCTAA GCCCCTTGCT TAGGGATACC ACTTCCCCAT 1740
GCCCCCATCC TGCCCTGGCC CTGGCCCTGG CCCGTGTCCA CCCCATCTCA CTCTCTCATA 1800
CCCACAGCAC AGACCCAAGG ACTCTTCCTG TAGCTTGGAA GCTGCAAGCT ACACCACTGT 1860
AGGCACTCCT GGTGGGCCTT CTGGAGGAGA GGACCTGCCT GAACCCAGCT ACTCCTGGGG 1920
CTTGGAGAGT CCGCAGGTTA CATTCCTACC TGTGACCTCG TTTATCAGTG CTCTTATCGC 1980
TCTTATCTCC CAAGTCGTTC CTCCTAAAGA CCCCTCTGAA TCTACACATC CCAGGCCCCA 2040
ACACCCTGGG CTACAGCAAC TCCCCAACAC GCCATTCTCT TCTTTCTTCT AGCAGTTAGA 2100
ATCTGGGTGT GTTCTGCCTC CAGGAAGCCT CTCATATTAA CCTGGGCTAA GGTCTCTGCG 2160
GGCCTCTGCT CCCCAGCTTC CCTTAGGCCG GGGTGATTCA GGCTGGCATT GGCTGCTGCA 2220
CGGCTGCAGG AAACCAGCTG CATCTGTTGG AAGGTCCTTT GAAGTTTAAG TGCACAGCCT 2280
CCGAGCGCTG GGGGCGGGGA CTGCTCTATC TCACCTAAGC CTAGGGCCTG CCCCTGGGTG 2340
AAGCCATGGT CACCCTCCCC ACAGCAGGAA CCACAGGCAG TATGACACAG GGTTCACCTG 2400
CGTCTTTTTC TATAAATATA GAAAAATGGA ATTATTTATT CAAATAATAA CTCTATTGAT 2460
ATGCTCTCAT TCCTGTTTGT GGGGAAGCCC CAGATGACTG TGTGGGTAAG TTACTATGGT 2520
ACGTAAGCCC CACCGTAGCC TGGGCCTGCA CTGCTCTCTC TGCATGTCAG TGAACTGCAT 2580
TGACACTGCA GGCCTAGTGA CAGGCAATGT CATCCCCATT TTACAGATGG CGAAACTGAG 2640
GCTGGGTGAA ATTAAAGGAC TTGGCCACGC TCAAACAGAC AGGAAATGGC AGAAGCTGGC 2700
CTGCCTGGTG CAAAAGCCAT ACAAAACTGA AAAGGACCTA ACACCGTTCT TGCCACAGCT 2760
GTCTAGGCCC CAAGCTCAGC 2780