EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS059-24947 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr2:43420040-43422810 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12614953chr243421461hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:43422786-43422804CTTTCTTTCTTTCCTTCC-6.95
EWSR1-FLI1MA0149.1chr2:43422790-43422808CTTTCTTTCCTTCCTTCC-8.46
Gata4MA0482.1chr2:43421880-43421891TCTTATCTCCC+6.62
PAX6MA0069.1chr2:43421205-43421219CCCTCATGCGTGAA-6.06
RARAMA0729.1chr2:43420740-43420758CACTGACCTGCTGACCTT-6.26
TCF7L2MA0523.1chr2:43422153-43422167GTCCTTTGAAGTTT-6.1
ZNF263MA0528.1chr2:43422786-43422807CTTTCTTTCTTTCCTTCCTTC-6.02
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
AAAGGCCAGC TCCATGCCCA CCTCCTCCAA GAAGCGCCAG CTGCTGCCCC CAGGCCAGCC 60
TCCACCTGCT CCCACAGGCT GGGGAGTGGT CAGGGAGGGT TTGCAATGTC CAGCTGCCCT 120
GTCTCCTGTC CCAGGCAGCG ATGTGTCCAG GGCTCCATAC CAGCTCCAAG CTCTCTGCCT 180
ACAGCTCCCT CACATCCACA CTCACTGGGT CCCAGCTGGA GACCTGGTGG CTTTGAGAGG 240
ATACCGTGGC TTCTTGATGT ACCTGAAGAC TTTGGAACGC CAGAAGTGTT CAGTCCTGTG 300
ATGGGTGTCA GCCAGGCCCA GAAAGCACAC AAACTGGGGG ACACATATGC TAAGTTATCC 360
AGAAAGCCTC AGGGCTGGGG CTGGAAGAGG AGGGCCTTGC CATCCCAAGG TGCTGGTGTG 420
TCCACACGCC CCTGGGGTGA CCGTGTGCAT CTGTGTGTGT GTGTTTGTGG GTGGGTGGCT 480
GACTACTCTG AGTTTGTGGG TGATTCATGT GTACCCTCGC GACAGGCTGT GTTCAGATAG 540
TCTGCTTATG TGCTTGAATT CAAGGACACA AACATCCCTA GGTGCAAGCT TGCACGCACA 600
GTCCTCCCTA CACCTCCACA CGCAACTCCT AATCATCCCT CAGGATCCTC TCCCCGCCCT 660
GCTTCAGCCT TAAGGCCTGC TCTGACCCTC CAGCCCATCC CACTGACCTG CTGACCTTCA 720
TCCCAGACAC TGCTGGGTTC AGCCCTGGAG CCTGGTCACT CTTGCTCCCT GAGGGTGAGG 780
TTGACTCCTT TTTAAATTAC CCCTAAAGCC CCACTTAGGG AGACACAGCC TTATCAATCA 840
ACACTCCTTG AATGAATTAA AACAAACTCC AAGGAAAGGA ACTGCATTTG GGTGGATGGA 900
AACAAGAGCT CTCAAGCTGT TTTCTTTCCT CTTTACCCTT TGCTCTCTGT CTCTTCCCAT 960
CTGTACTTTC TCTAACTTGT TTGCTAACTC AATCGTCAGC TTAGAAAGTA CTTCCTTGTA 1020
TACCCTCCTC TCATTCAAAT CTCATGACAA TCCTCCAAGA CACGAATAAT TATCCTCATT 1080
GCACAGATGA GGAAACTGAG GTTCAGGGAG GCTACGTGAG TTGCCCAAGG TCACACAGCC 1140
TGGAAGGAGT GGGTAGGGAC TAGAACCCTC ATGCGTGAAT GGACACCACC TCCCACCACT 1200
CCCCACCAGT AAGTAGAGGG TGGAGGGTAA AGGGCGATCC AGGGGCTCGG AGAGGATTGG 1260
CCTCTTCAAG CCCTCTCCAT GGCCCAAGGT CACCGTGGGA GGGAGATGCA CCTGGCCCCC 1320
AGGGCCAGGG GTTACCCCAC TCGGCCAGCA ATGGGAGAGG CCATGAGATC TGTGGACATT 1380
GTTCCTGGGC CTGTGGTTAC TGATTTGACA ACAGCCCTGT TCCTCCCCAG CCAGCCAGGG 1440
AGTTAATGAT TAAGGAGGAG ATTAAATATT AACCACCTGT GGGGCCACGG CGTAATGTCT 1500
CCATCTGCAC CTGAGCCTAC CTAAAAATCC CTCCCACCTG CCGTGGGCCA GCCCCACACA 1560
GGGCCTCTAA GCCCCTTGCT TAGGGATACC ACTTCCCCAT GCCCCCATCC TGCCCTGGCC 1620
CTGGCCCTGG CCCGTGTCCA CCCCATCTCA CTCTCTCATA CCCACAGCAC AGACCCAAGG 1680
ACTCTTCCTG TAGCTTGGAA GCTGCAAGCT ACACCACTGT AGGCACTCCT GGTGGGCCTT 1740
CTGGAGGAGA GGACCTGCCT GAACCCAGCT ACTCCTGGGG CTTGGAGAGT CCGCAGGTTA 1800
CATTCCTACC TGTGACCTCG TTTATCAGTG CTCTTATCGC TCTTATCTCC CAAGTCGTTC 1860
CTCCTAAAGA CCCCTCTGAA TCTACACATC CCAGGCCCCA ACACCCTGGG CTACAGCAAC 1920
TCCCCAACAC GCCATTCTCT TCTTTCTTCT AGCAGTTAGA ATCTGGGTGT GTTCTGCCTC 1980
CAGGAAGCCT CTCATATTAA CCTGGGCTAA GGTCTCTGCG GGCCTCTGCT CCCCAGCTTC 2040
CCTTAGGCCG GGGTGATTCA GGCTGGCATT GGCTGCTGCA CGGCTGCAGG AAACCAGCTG 2100
CATCTGTTGG AAGGTCCTTT GAAGTTTAAG TGCACAGCCT CCGAGCGCTG GGGGCGGGGA 2160
CTGCTCTATC TCACCTAAGC CTAGGGCCTG CCCCTGGGTG AAGCCATGGT CACCCTCCCC 2220
ACAGCAGGAA CCACAGGCAG TATGACACAG GGTTCACCTG CGTCTTTTTC TATAAATATA 2280
GAAAAATGGA ATTATTTATT CAAATAATAA CTCTATTGAT ATGCTCTCAT TCCTGTTTGT 2340
GGGGAAGCCC CAGATGACTG TGTGGGTAAG TTACTATGGT ACGTAAGCCC CACCGTAGCC 2400
TGGGCCTGCA CTGCTCTCTC TGCATGTCAG TGAACTGCAT TGACACTGCA GGCCTAGTGA 2460
CAGGCAATGT CATCCCCATT TTACAGATGG CGAAACTGAG GCTGGGTGAA ATTAAAGGAC 2520
TTGGCCACGC TCAAACAGAC AGGAAATGGC AGAAGCTGGC CTGCCTGGTG CAAAAGCCAT 2580
ACAAAACTGA AAAGGACCTA ACACCGTTCT TGCCACAGCT GTCTAGGCCC CAAGCTCAGC 2640
TTCTTTTCAG CCACAGTTCC CAACCATGTG TGGCTTGCTT GCTTTTCTTT CTTTCTTTCT 2700
TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCC 2760
TTCCTTCCTT 2770