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

TagContent
EnhancerAtlas ID
HS076-31671 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr2:42327990-42330610 
TF binding sites/motifs
Number: 15             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELK4MA0076.2chr2:42329937-42329948GCACTTCCGGC+6.14
FOSL2MA0478.1chr2:42328239-42328250GGGTGACTCAG+6.02
Foxd3MA0041.1chr2:42330441-42330453GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr2:42330445-42330457GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr2:42330449-42330461GTTTGTTTGTTT+6.32
JUNMA0488.1chr2:42329278-42329291TAAATGATGTCAT+6.67
JUNBMA0490.1chr2:42328239-42328250GGGTGACTCAG+6.02
JUND(var.2)MA0492.1chr2:42329277-42329292TTAAATGATGTCATC+7.09
KLF16MA0741.1chr2:42328455-42328466GCCCCGCCCCC+6.02
KLF5MA0599.1chr2:42328455-42328465GCCCCGCCCC+6.02
Klf12MA0742.1chr2:42328292-42328307AGGCTGGGCGTGGCC-6.01
MAXMA0058.3chr2:42329397-42329407ACCACGTGCT+6.02
PLAG1MA0163.1chr2:42328804-42328818CCCCCGACGGCCCC-6.33
RREB1MA0073.1chr2:42329770-42329790CCCCCCCCCACCCCACCCCG+6.95
RREB1MA0073.1chr2:42329775-42329795CCCCACCCCACCCCGCCTCA+6
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_00451chr2:42323824-42331106Adipose_Nuclei
SE_10312chr2:42325221-42336343CD19_Primary
SE_11146chr2:42323572-42336874CD20
SE_11946chr2:42327841-42337002CD3
SE_14693chr2:42327772-42338606CD4_Memory_Primary_7pool
SE_16102chr2:42328229-42330615CD4_Naive_Primary_7pool
SE_16740chr2:42328038-42330759CD4_Naive_Primary_8pool
SE_16987chr2:42327433-42336274CD4p_CD225int_CD127p_Tmem
SE_17444chr2:42325062-42338640CD4p_CD25-_CD45RAp_Naive
SE_17811chr2:42325303-42338643CD4p_CD25-_CD45ROp_Memory
SE_18685chr2:42325197-42338156CD4p_CD25-_Il17-_PMAstim_Th
SE_19964chr2:42327606-42335969CD4p_CD25-_Il17p_PMAstim_Th17
SE_20190chr2:42327806-42336196CD56
SE_21801chr2:42328127-42336332CD8_Naive_7pool
SE_22420chr2:42327613-42337810CD8_primiary
SE_30543chr2:42327857-42328518Fetal_Muscle
SE_30543chr2:42328585-42330631Fetal_Muscle
SE_43599chr2:42327765-42335085MM1S
SE_50137chr2:42325319-42330465Sigmoid_Colon
SE_53105chr2:42327856-42330509Small_Intestine
SE_53609chr2:42323895-42330707Spleen
SE_55583chr2:42328464-42330317Thymus
SE_62313chr2:42323195-42370065Tonsil
SE_67366chr2:42327765-42335085MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr24232820042328478
Number: 1             
IDChromosomeStartEnd
GH02I042097chr24232414142336955
Enhancer Sequence
CCCTAGAAGC CGACTCCGCC TGGCCCACCA TGCCTGCAGC AGAAAGGCCT GAGGCTGGGC 60
CTAGAACACT GAGGACGTCA GTGGCCAGGA CTTTCCAAAG CTGAAACTGG GACCTGCGGA 120
GGCCTCACTG TCCGGAGCAG CGTCCAGGTC CTCAGCATCC TCTTCGCTGG GCCCCACGCG 180
TGTCGTGCGC CACCCCAGAA GGCAGGGCCT GATTCGGATC AGCAGGGGCT GCAGGGCCGC 240
TCTGCAGGTG GGTGACTCAG GCCCCTCTTG AACCCTTAGG CCTGAGGCAG AGACTGGGCA 300
GGAGGCTGGG CGTGGCCGGG GAGCCCCTTC ACGTGCTCCC CTTCTCGAGG GTTCACGGGG 360
CTCTGGAGGC CCAGATGCTG GCAAAGTGGC GGGAGCGCTC CAGGGACGAG GACTCAGGTC 420
GGGGCGCCCC CGCCAGCGCC AGGATCCCCG CTCACCCTCC GCCGCGCCCC GCCCCCGCCC 480
CGACACACTG GGGGAGCCCC GCCCTCCCCG AGGCCCGCGC GGCGCCGCAG GAGGAATCCC 540
AGCCATTTCC TCCACGCTGC GCGGTATGTG GCCTGCCCGC CGCCAACCGC AGCGCGAGCC 600
GGTCCCCAGC CGCGCCTGGC AGCTGCCCCG GCTCCGCCGT GCTGCTCGGG ATTCCGGGAA 660
GGCCGCCCCC TCGTCCCGGG CCACCAGACC GGCCTTTCCA GCGGCTCCAG GCCCGTGCAG 720
TCCCGCCGGA CGCCGGCTAC ACCACGCGCC GCTGCTGGAA CCTCTCCCAG CCCCGCGTGG 780
CCGCCCCCGG CCCAGGCACC CCCTCCCCGG AACGCCCCCG ACGGCCCCTC GCGTCCGAGC 840
TGGAAACTGA AGTTGACGCT TGCTCCGTCA CCCTGGGGCA AATTGCTTTG CCTAAGCCTC 900
AGTTTCTCCA TCTGTGAAAT GGGGACGTTG GCAGGAGTGC CTGTCTCGTT GTGCTGCCCG 960
AGGGGTGAAT GAGAAAAGGA AAGCGTTGGA CTACTGTCAA CGCGATTTTC ATTTCCCTAG 1020
GTACCACGAG GGTCCTGGCT TTTCGCACAG GATCTTAGCA CCCACCCTGC CCCTCGCCTC 1080
TCCTCCAGCC CAGTTGCCGG TGGAGCAAGC AGGCCGGGCT TTGCGAGTGG GCAGAGGAGA 1140
GGGCTGGGGC CTGCCCAAGA CTGCGCCCTG CACAGATTAA ACAATGCCTG AAGGTCCCAC 1200
GACACAGCCT TCCTCGAGAT TCACCGTTGC CCTCTCCTCA ATCACTAGGT TCTTGAAAGA 1260
CCCAAAGGAC AGTTATTTAC ATTTTTTTTA AATGATGTCA TCGCAGTCTG AGAGCAGCCA 1320
GACACGTAGT GATCAGGGAA AGTCGAAAGT GCAGATGGGT TCGCAAACGT GGACTCTCTA 1380
GTTTTGGGTC TGCAGATGGG GCCGGCCACC ACGTGCTCTC TGAGTTCTCT TTCCAAGTAC 1440
AGATCCCTCC GGAGACGGAA CATTGTTCCG CCTTTAATTC TTCCCAGGAG CTGCGGAGGA 1500
AGGCGTGAGA ACCGGAGCCC GGGGTGACTT GCGGGGGAGG GGATCGCTTC CCCGTCGCCC 1560
ACACCTGCCT AACCCACGCC CACGGCGGCC GCAAAGGCGA CACCGCGTGA ATCTGGAAAG 1620
CCCCGAGTTT CAACAGGCCC AACCATCGGC GGCTTTGCAG GCGCAGCACC AAGTGCTGCT 1680
CTGCCTGTGT TCCCCCAGAC AGCCCCTGGT TGTGATTTGT CGTTTCCAGT CCAGCTAGAG 1740
TCCCAAGGCC AAGAACTAGA CCCTTGCAGC GAGATCCGCG CCCCCCCCCA CCCCACCCCG 1800
CCTCATTCTC CACAGGCGCC ACAGCCACAG GCCGCATAAA TAAATCCAGG TGGAGGCAGA 1860
CCCAGAAACC CAGGTGCTAT AAATATCCCA GCCCAGCCGG GAGACTGACC TCCCAGGCAG 1920
CCCCTCGCCC CCACCCGCCC TAGACCAGCA CTTCCGGCCA CCACAGCGCT GAGGGCGGAT 1980
CTCCCCGCGG TGGGAGGAGC GGGCTCCACC AGGATGCAGG CCTGGCTTCC CTTTCTTTCT 2040
TCTCCTGGGA GCCTCTGGCG GCCCAACCTG AGGGCTTGCC CTCTTCTCTG GAACCACCTC 2100
CCTAACTCTC AATCGCATAC CTCTCCCTCC CTCCCCCTGG TATTTTTAGA GAGGCCTTCT 2160
CTCAGGGACC CCATACTGCG ACCAGACTTC AAGAAATGCT GACTTCTCTT TCTAGATGAA 2220
TAAGCATAGT TGGAAGGCAA CAACCTCAAT CAGAGTTTAC AATCTAAAAT TTGATTCTAA 2280
ACTTTTTCTT TTTGAAACAG TCTTGCTCTG TCACCCAGGC TGGAGTGCAG TGGCGTGATC 2340
ATGGCTCACT GCAGCTTTGA CCTCCCAGGT TCAAGCGATC CTCCCATCTC AGCCTCCCTA 2400
GTAGTTGGGA CTACAGGCGC TGTGCCACCA TGCCCGCCTG GCTAATTTTG TGTTTGTTTG 2460
TTTGTTTGTT TTTGTTTTTG TTTTTTTTTT TGAGACGGGG TTTCACTATG TTGCCCAGGC 2520
TGGTCTCGAA CTCCTGGGCT CAAGCGATCT GCCCACCTCA GCCTCCAAAC ATGCTGGGAT 2580
TACAGGTTTG AGCCACTCTG TCCAGCCCTT GATTCTACAT 2620