EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-10674 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr15:40384580-40386810 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr15:40384902-40384917TAGGGGCAAAGTTCA+6.41
Hnf4aMA0114.3chr15:40384903-40384919AGGGGCAAAGTTCAGG+6.42
MAFFMA0495.3chr15:40384597-40384612CTGCTGAGGCAGCAA-6.18
MAFFMA0495.3chr15:40384597-40384612CTGCTGAGGCAGCAA+6.21
MAFGMA0659.1chr15:40384594-40384615ACACTGCTGAGGCAGCAAAAA-6.34
MAFGMA0659.1chr15:40384594-40384615ACACTGCTGAGGCAGCAAAAA+6.76
MAFKMA0496.2chr15:40384595-40384614CACTGCTGAGGCAGCAAAA+6.26
SOX10MA0442.2chr15:40384839-40384850AAAACAAAGAA+6.62
TBPMA0108.2chr15:40384724-40384739CTGCCCTTTTTATAG-6.07
ZNF263MA0528.1chr15:40385773-40385794CCCCCTCTCCTCCCCTCCCCA-6.19
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_02129chr15:40384673-40385638Aorta
SE_09809chr15:40384570-40394646CD14
SE_10247chr15:40384267-40394494CD19_Primary
SE_10901chr15:40379120-40402300CD20
SE_24160chr15:40385139-40385649Colon_Crypt_2
SE_28229chr15:40383525-40386111Fetal_Intestine
SE_29542chr15:40383741-40386086Fetal_Intestine_Large
SE_30713chr15:40383810-40385991Fetal_Muscle
SE_31657chr15:40384600-40386298Gastric
SE_32631chr15:40385680-40400407GM12878
SE_33749chr15:40383375-40394469H2171
SE_37146chr15:40382763-40387193HSMMtube
SE_41090chr15:40384226-40386245Left_Ventricle
SE_41752chr15:40384462-40385656LNCaP
SE_42538chr15:40382887-40388290Lung
SE_46900chr15:40384760-40386080Ovary
SE_47647chr15:40384952-40385677Pancreas
SE_49093chr15:40383872-40386228Right_Atrium
SE_50219chr15:40383292-40386988Sigmoid_Colon
SE_51397chr15:40384311-40386450Skeletal_Muscle
SE_52941chr15:40383696-40388761Small_Intestine
SE_54376chr15:40383347-40386447Spleen
SE_58347chr15:40336303-40409644Ly1
SE_58853chr15:40336022-40409018Ly3
SE_59746chr15:40336643-40415102Ly4
SE_60404chr15:40336144-40409045DHL6
SE_61090chr15:40336308-40414973HBL1
SE_61688chr15:40336793-40410942Toledo
SE_62368chr15:40336601-40408809Tonsil
SE_65648chr15:40384400-40386217Pancreatic_islets
SE_68227chr15:40361115-40402006TC32
SE_68538chr15:40360882-40401938TC71
SE_69122chr15:40382944-40385992H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr154038557140385715
Enhancer Sequence
CTTCAATTTA AACCACACTG CTGAGGCAGC AAAAATCTGA TTTCATCCAG TGCAAACACG 60
CACACACACA GACTCACACA CACACACACA CACACACCCT TGTGCGCCCG CCCGCTCTCC 120
CTCCCCAGCA TCTCCAGCTC GGTGCTGCCC TTTTTATAGA TGCTCTTGAC AGTAAGCCAT 180
AAATAATCCC TCTTGGAGCG CTCTCCTACT GACTGGAGCC AATTAAACAT TAAGCAAGAA 240
CATACTTGAA AACAAAACAA AAACAAAGAA TATATACTAT GCTCTGGAGG TTATCCCAGG 300
TCCTACTGTC AGGCTGGGAA GCTAGGGGCA AAGTTCAGGG GTCAGTGGCT CACCAGATTG 360
GGGCTGGTGC CCTGCCCACA CAGGTACCAT TTCCCAGGAG AGGCCTGGGG GGGTGGAAAC 420
TGGGGGGTGC TGGAAGAGGC GGTCTTTGTT CTCTCTTTGT CTGCCAGGGC AGGAGGACTG 480
GGCGGGGGCC TCTCCACAGG GTTCTCACTG GACAGGGGAA TAAAAACCTA GTGTGCAGAA 540
AGGAGCCAGC ACGGGCTGGA CTTGGATTAC TTCAGTGGCC CCGTCAGCAA GCAAGTTTAC 600
ATGAGGTGTC CAAGCCTTCT CTTAAACTGT CTTTAACCAC AGCACCAGCC CCCACCAGGC 660
AACTACTCCT GGTCAGATGG GAAGAGGAGA GAGGAAGCCA GCGGCACAGC TGGAAAGGGG 720
GCCCAGGTTG CCTGGACTCC CAGAGCTTCC AGGTTCTGTC CAGCCCTGGC CTCCCTGACC 780
TTTCCCAGGG CCACCATGCA GGTTGCTGGC TTCCCCTTCA CGCTGCCCTA GGCCACAAAA 840
AGAGAGGCAT CCAGGCAGCT GGCCTCAGGG CCTGACAACC CAGGTGAACA CGGAATGCCC 900
CCGTCCATCA TGGCAACAGC ATTCCTCCTT CCCCCGTGGA AGAGCCTGGA AAACAACCCG 960
GCAAGCTGGA GGCGCAGCTC CTGCCCGGAG GGGAAGGGAA ATCGGGCGTG CCACAGAAGA 1020
GGCCTGGCAG ACAGAGGGTG GGGAGATGGA TGGCTTCCTC GTGTTTTGTA AACAAAGATG 1080
AGTAAAAAGA GGAAACACAC CCGGCTTAAC AAAATCTGGT TAGAGTAAAA CAGCGTGAAA 1140
ATGGACTCAG CTGCAAACCC GAAGCCTCCG GCCTGCAGCA GCTGGGCCAA AGACCCCCTC 1200
TCCTCCCCTC CCCAGCTGCT GACCGAGACA GGTGCAGAGG TCATGTGGCC GAACAAGAGG 1260
AGAATCCAGG AGCAGACTCA TCCCTGGAGA GGCCAGTCTG CTGGAATTCC AGTTCTCCTG 1320
AGGTGCTTGT CTGAGAAGAC CGGTGGCAAG AACAATCATC ACCTCATAAT AGTAACGTGG 1380
GGTTAGGGTG GCAGTCGGGG GTGGGGAGGT GCCAGGCTCT GTTCTGTGTG TTCTGCATCC 1440
TTGCTTCTCA AAGGGTGGTC CATGGACTAG CAGCCTCAGC ATCATCAGAG AGCTGCCTGG 1500
AAATGCAGAC CCAGCATCAG AAGATTCCCC AGGTGATTTT GAGGCACATT ATCATGCCCA 1560
TTACTTAGCG ACCACATAGC TAGTTTAAGT GGCAGGGACT GGACTGAACC TAGACCATCT 1620
GGCCCTAGAG CTATGTCCCT TCCCATTATC TCTGTGCTCA GAGTGCCACT ACCTTTCTTT 1680
ATACCAAAGC AGACCCTCTA GCCTCCCCTT TACTAAATCA TCTCAAAACA GCTCAATGGC 1740
CAAGGAAAGC AGATGAGAAT TCTATGATTT GGGGCTGAGG CAATTCTCAT CTCTGTATGC 1800
CTCAGTTTTC TCCCAAATTC CACTAATGGA GGCCACCTAC TCCCTGGGCA ACTTGAGATC 1860
TCTGAAGATG AGGCACAGAC TCCCATCATC TGGGAGCGTT GGGGGACTCA GAAGCAGCTG 1920
TGGGCCAGAG AGTGCTTTCA GACAGGAAGG CTGAGGTCTT GCAGGGGACC CAGGCAGGCC 1980
TAGGTGCAGG AGGCAGGATA CATGGGCCGG CCCTTGGGAA GGAACTAGTT TCCATGCCTC 2040
TGCGTGTGAC AGTCCTTAAG GCTCATGAAT TGGTAAGGAA GGCTCTATGG TGCATGGATC 2100
CCCAGGGACC AGGAATCAGA GGACCTGGCT TTCGGGTTGG ATCTCCCATC AACCTGCTCA 2160
TGAGTTCTCT CTTGGCTTAT AAGGAAAATG CAGGTATTGT ACTAGATCAA TGGTTTCTAA 2220
ACCCAACTGT 2230