EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS156-06871 
Organism
Homo sapiens 
Tissue/cell
P493-6 
Coordinate
chr2:30446030-30448930 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:30446035-30446053GGGAGGAAGGAAAGAAAT+6.26
EWSR1-FLI1MA0149.1chr2:30446031-30446049GGAAGGGAGGAAGGAAAG+8.96
Foxd3MA0041.1chr2:30447449-30447461GTTTGTTTGTTT+6.32
IRF1MA0050.2chr2:30448229-30448250AAAAGAAAACTGAAAGTGCTT-6.87
RORA(var.2)MA0072.1chr2:30446633-30446647TTGACCTACTTAAC-6.76
SPICMA0687.1chr2:30446590-30446604AGAAAGGGGAAGTC+6.23
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01755chr2:30446105-30447496Aorta
SE_01755chr2:30447563-30450645Aorta
SE_11970chr2:30444665-30450778CD3
SE_14558chr2:30446217-30450315CD4_Memory_Primary_7pool
SE_15685chr2:30445830-30450089CD4_Memory_Primary_8pool
SE_16004chr2:30447413-30450236CD4_Naive_Primary_7pool
SE_16644chr2:30445645-30450422CD4_Naive_Primary_8pool
SE_17225chr2:30446071-30447344CD4p_CD225int_CD127p_Tmem
SE_17225chr2:30447557-30450049CD4p_CD225int_CD127p_Tmem
SE_17384chr2:30445212-30451927CD4p_CD25-_CD45RAp_Naive
SE_17932chr2:30443982-30451020CD4p_CD25-_CD45ROp_Memory
SE_18365chr2:30444935-30451821CD4p_CD25-_Il17-_PMAstim_Th
SE_19353chr2:30444534-30450722CD4p_CD25-_Il17p_PMAstim_Th17
SE_20596chr2:30444335-30450690CD56
SE_21342chr2:30445106-30450334CD8_Memory_7pool
SE_21674chr2:30445866-30450369CD8_Naive_7pool
SE_21992chr2:30446025-30450837CD8_Naive_8pool
SE_22456chr2:30444196-30451537CD8_primiary
SE_30975chr2:30442683-30450154Fetal_Thymus
SE_37161chr2:30447758-30450479HSMMtube
SE_38909chr2:30447739-30450059IMR90
SE_40870chr2:30446088-30447510Left_Ventricle
SE_40870chr2:30447555-30449501Left_Ventricle
SE_42426chr2:30446157-30447463Lung
SE_42426chr2:30447572-30450052Lung
SE_50508chr2:30445470-30450398Sigmoid_Colon
SE_52885chr2:30445505-30447543Small_Intestine
SE_52885chr2:30447666-30450492Small_Intestine
SE_53678chr2:30445514-30450413Spleen
SE_55218chr2:30445375-30447505Thymus
SE_55218chr2:30447691-30449522Thymus
SE_62379chr2:30440168-30517171Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr23044812530448425
Number: 1             
IDChromosomeStartEnd
GH02I030221chr23044428830450540
Enhancer Sequence
AGGAAGGGAG GAAGGAAAGA AATGGTATGC CCAGATCTTT TTTCCCCTCT TCTGAGTTAA 60
ACAGCTCAAG TGCTATGATC ATATTAGATC TAGGGACAAG AATTCCAATC AGATCCCTCC 120
AGAAGGACTG TGATGGACAA GGAAAGTCAC CTCATACTGT GCCCACTGGA TGCACCCACC 180
CCAGCCCTTC CAGGTGGTTC CCCCTCTCTC TCTCATCATG ACATGGTTTC CCCCTGGGCT 240
TCAACCATCA ACCATCAATT TGCCTCCAGG ACCAGAGACT TTCCTGTCAC CCACTTACCC 300
TGTCTGCAGT GCCACCATGA AACTGAGGCC TTTGAGGTGC TGCCTGCATG TCATTCTCAC 360
AATAGTGTGA ATTCATTTGT CAGATCAAGT TCTCTTGCCT GGCAGCTGCC TTGGCTTAGA 420
GAGCTGCAGG ATGGAAGTTT CAGTGGAAAA GCAAAGAGTG GTTTTGGAGC TTGGGAGGCT 480
GTTATGAAGG GAGTGTGGGG CTTCCTGAGT TCAGTGGGTG CCTGGGGCGC ATTGAAGGGA 540
AGTGTGAAAC AAGAGGGGTT AGAAAGGGGA AGTCTCAAAA GACAAATTTC ACATACATGA 600
AATTTGACCT ACTTAACACT TCTGCTGAGG CCCCACCTGG CTGGAAGAGA AACGCTGATA 660
TTAACTCGAA TAACATAGAG GTGAAGGAAC CTGGACTGAT TTGGCTAATG GAAGTAACAG 720
ACTTTTCTTT CTGCTAGAAA TTGTGTGCAC AGTCCCTTCC GCAGAGCATG AGGCCTTTTA 780
CTCACAAATA GTTATTCCCT TCAGCATGTA GACTTGGAGT CATGGGAGTG CCTCTCCCAA 840
GGTCTGGAAT AGATAATGCT GCTGCCCACC CCTAGTTCCT GGGACACACC TGGCCCTTTC 900
TGACCCCTAC ACCTTTGCTG ATGTTGTTCT GCTGGCAGGA TCGCCCTTCT CTAGCTTCTC 960
CCCATCCTTT GAGGCCAGCT CAGTTGCCAT CCCTTCCCTT TAGCTATTCC TGCTACCATT 1020
CTTTCCACAG ATATTCCCTG AGTGCCTGCT AGATTCCAGG CACTCTTCTG GTGGTGGTGA 1080
CACAGTAAGA CACAAAACAG ACCTACTCCT TGCCCTTGAG AGCTTCCCTT CTGCCAGTCA 1140
GCCCCCCTCT CCCAGTGCCT TTGCCTGGGA CTGAACTAAT CATATCCCCA CCCATGCTCA 1200
CATGAGTCTA CTGCAGCAGT TATTGTATGA TATTAGAGGG AGTGGCAACT AGGTTCCCAG 1260
ACACCCCAGT GCCCAACACC TTGCCAACAC CAGAGGTAGA CTCTCACTTC TTTAAAAAAG 1320
AAACTCAGGG GTAGCAATTT GCATAGGAAG GGCAGAGGCT AGGAGACTTA CCTGCAAAAT 1380
GCACTTGCTA GCATGTGTGA CCGTTCTACT TAGTTTTGTG TTTGTTTGTT TTTGTTTTTG 1440
TTTTTTTTTT TGAGACAGTT TTGCTCCGTT GCCCAGGCTG GAGTGCAATG GTGCGATCTC 1500
AGCTCACTGC AACCTCTGCC TCCCGGGTTG AAGCGATTCT CCCTGCCTCA GCCTCCCAGA 1560
GTAGCTGGGA TTACAGGCAC CCAACACCAC GCCTGGCTAA GTTTTGTATT TTTAGTAGAG 1620
ATGGGGTTTC ACCATGTTGG CCAGGCTGAT CTCGAACTCC TGACCTCAGG TGATCCGCCC 1680
ACCTCTGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGTGCGCG GCCTTAGTTT 1740
TGTGATTCTT TGAGGGGATC ATTAATGCAG TTTAGGGAAT TTGTCTTACA GGTGCAGTGA 1800
CCTTGCAGGC ATAATACCAT CACACAGACT GTGGTTATCT GGGATGGTTA CAGGGAGTTA 1860
TGGAGACAGG AGAAAACTAA ACGTCTCCTA AACCGATTCT TTGGAAATGC CAGCACCTGT 1920
CTGGCACACA GTGGGTGCTA ATGCCTGTTA GAATTGTTGT TGAGAGGGCA GGAGGGTGTA 1980
ACATGGACCC AGCTATCTGA TCCTGAGGCT GGGCGCCATG TGGGTGTGAA GTACACCAGG 2040
GGCTCCAACC AGCAAGTGCT AGCTCAGGTT ACAGTTAGGG AGCTGGCAGA GTGTTCAGGA 2100
GGAGCTGCTG TCTGGTGCAT AACACGCAGC TCGCTCCTCC AAGGAAGAGC AACAACACAG 2160
CTGCCCCTGG AGGAAGCTAG CAGACATCCT GTGTACTTGA AAAGAAAACT GAAAGTGCTT 2220
TTCTTCACAA GAAACTGTTG TGTTTCCCTC TTTTTCATAA ATCCTCCTCC CTCCCCTGCC 2280
GCCCCAGGTA TGATGGAGTT TCCCTGGTCC AGAGTTGTGG GTAAAATAGT GGGAGACGTG 2340
GACAGAGTGG TATGAAGGGA GTTTATGCTG GGCTGTGGTC CGTGCTGTTT GTCTAATTCA 2400
GGGAAGGTAT CAGGCTACCC CAAGGAGGAC TCTGCTATAC GATCTGCATC CTGGTGATAG 2460
TAACCTCTCT TTTCTGGCTG TTGAAGTGCA TTCCTGTGCG GATGTGGAAA GAGAGAAAGC 2520
AAGATACAGC CAGGGCTAGG ACAGGAATGT GAGTATTTCC TTAATTGGAC ATGAGAGCCT 2580
TGAACTGATT CCAGTTGGAG TGTTTTCTTT TAGGGCCTGG ACCCTAAAGA TTTCATACAG 2640
TTTTCTTTGT CAGAAAAATC CCTTTGGTTC AAAGGCCCCT CGATAGAAAT AAAGAAAAAG 2700
CCAGGGCTGA ATTTCTTTGA TATGTGGGAA GGCAAGAGTT TATGAGCTGC CAGATCTCAG 2760
GCTTCTTTTG GGGGCAATGA GAGGATTCTG GACTGAAAGA TGAAGGCGCC TCCTGCGCTG 2820
CCACATGGGA AGAGGGACCA CTGGCTTTAG GGTGGGCTGC AGAGCCCCAG TGGTATGGTA 2880
AGGACGTAAA GCACTTTTCT 2900