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

TagContent
EnhancerAtlas ID
HS047-08613 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr12:111862460-111864840 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11065898chr12111862575hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr12:111862612-111862627TGACCTCTGACCCAG-6.85
Nr2f6MA0677.1chr12:111862612-111862626TGACCTCTGACCCA-6.37
RREB1MA0073.1chr12:111863055-111863075GGTGGGGGTGTGGGTGGAGG-6.03
RxraMA0512.2chr12:111862612-111862626TGACCTCTGACCCA-6.12
ZNF263MA0528.1chr12:111864353-111864374GGAGAAGGAGGGTGAGAGAGA+6.79
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00313chr12:111862498-111864730Adipose_Nuclei
SE_09337chr12:111861899-111889874CD14
SE_11164chr12:111861758-111877253CD20
SE_11924chr12:111863179-111876859CD3
SE_13643chr12:111861951-111863542CD34_Primary_RO01536
SE_14612chr12:111861870-111865360CD4_Memory_Primary_7pool
SE_15617chr12:111864113-111865098CD4_Memory_Primary_8pool
SE_16453chr12:111863807-111865126CD4_Naive_Primary_8pool
SE_17009chr12:111863355-111864997CD4p_CD225int_CD127p_Tmem
SE_17538chr12:111862008-111876816CD4p_CD25-_CD45RAp_Naive
SE_17816chr12:111861604-111877277CD4p_CD25-_CD45ROp_Memory
SE_18496chr12:111861894-111877196CD4p_CD25-_Il17-_PMAstim_Th
SE_19231chr12:111862803-111865000CD4p_CD25-_Il17p_PMAstim_Th17
SE_20028chr12:111861972-111865042CD56
SE_21344chr12:111863969-111865359CD8_Memory_7pool
SE_22364chr12:111862617-111877141CD8_primiary
SE_24616chr12:111862648-111863788Colon_Crypt_2
SE_24616chr12:111863791-111864106Colon_Crypt_2
SE_24616chr12:111864227-111864966Colon_Crypt_2
SE_32074chr12:111862890-111863980Gastric
SE_38040chr12:111862345-111877177HUVEC
SE_40041chr12:111863639-111864112K562
SE_40792chr12:111861955-111865007Left_Ventricle
SE_42263chr12:111861812-111864991Lung
SE_46057chr12:111861628-111864964Osteoblasts
SE_47422chr12:111862028-111864740Panc1
SE_48851chr12:111861936-111864223Right_Atrium
SE_50268chr12:111861932-111865018Sigmoid_Colon
SE_52677chr12:111863051-111864959Small_Intestine
SE_53326chr12:111861897-111876991Spleen
SE_62745chr12:111834432-111886877Tonsil
SE_68830chr12:111861976-111863878H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12111862589111862884
chr12111863408111863975
Enhancer Sequence
GGGGAGGCTT CTCCTAGCCC CTCGGAGCAT CAGGTGGAAC AGTCCGGGCG GCTCAGGAGC 60
ATCCCCTCAG TGAATCTGTG TCCAGGTGAT GGGCCAAGGG TGCTCAGACC ACAACTCTTG 120
CATGTGCTTG CCAGGTAGTC AACTGTGATC CCTGACCTCT GACCCAGGGG TTGGCTCTGG 180
GAACAGTTTT AAACAAAAGG AAAAGAAAGT TCTGACAACC AGTGGGTGGT GGCGAAGGGC 240
TTAAGCTTTG GATCTGCACT TGCGGTCTGT CACTTAAAGG GTGCCCTGCA GGAGAGGGAG 300
CAGATGTAAT CCCAGTGCCA GCCTGGTGGA GGCCCTGCTG CCCAGGGCTG GAAGAGGCTT 360
TGGAGGGAGA GAGCCAAGAG AAGGCAGCTG CCCAGAAGTC TGAGGCCAGG TGGGCTCAGC 420
CCACAGGTGA GCCTCACCTG CAGTTGGGCC CCAGCTCTGC CCCCGACCTG CTGTGTGACC 480
GCGGGCCTGT GGAGCAGGGT GATGGTGTAG CACCTCCAGG GGCACTATGA GGGCTGCGCT 540
GGGAGAGAGC ACTCTGTGAC TGGGGGTGTG CAAGGGGAGG CCACAGTCTG CCAGGGGTGG 600
GGGTGTGGGT GGAGGAGATG TCTGTGTTTT CCAAGGTCAG GAGAAGGGGA GAAAAGTCCC 660
AGCTTTCTCT GGTCTCAGTG GCCACTGCAG GTGGGCAGCG TGGGCCCTTG GGAGGTGGGA 720
GGGGGCTGCC TTCCCTGGGG TTGGTCAGCA AAGGCCTCTT GGCAGGAGGT GCCGGTCCTG 780
ATAGATCTGG GTGAAGGAGT CCCAGGCTGA GGAATGGCAG GTTCACAAGC CCTGCAGTGA 840
GCGTGAACCA GGCAAGTCTG TGGAATAGCC AGGCAGCCTG GGGTTCGAGG GAACAGGGAA 900
AGGTGAGACT ACAAAGGTAG TGGAGCTGGA TTGCAGAGGC CCTTGTGGGC CACAGTGGGG 960
ACTTTAGGTT TTACATTAAG AGCAGTGGGA ACAATTGGAG GATTTAGGCC TAGAGGGCCT 1020
GAGACACTTG CTGGGGCCAC CTGCGGGTGG GAGTGGGTGC AAGGGACCCT CCAGGCTACC 1080
TGTGGTCTCC CAGCTCAGGC CCGCGATGGG AGAGTATGAC ATGATTTCCT CTAGAGACCT 1140
CCTTCCCCTG GGCACCGCTG AGCCCCAGGC AGGGCAAGGA CAGGGGAGCA GTGTGTTTAT 1200
GTGGGGGAAA GGTGACATGC CTTTCATCAC CCATCATCGG GCTCACGACC GACACTCTTG 1260
CAACAAGACA GGTCAGCAAG AGAAAAGCAT CACAAAGTTA TTGAATCAAA GTTTTATGTG 1320
ACATGTAGCT TTCAGGAATG AAGACCGAAA GACCCCAGGA AATGGTCTGT CTGGTGTTTA 1380
GGTTTGATGG AGCAGGGATA GCTGCGTAAA AATGGGATTG GGATGAAAGG GTGTGATCTA 1440
CTGAGCTAGA CGGAGGCGGG GTCCCAGCAA GGCCTGCTTG CTCCCATTCC TCTTGGCCTC 1500
TGCATGGTGT TCCTTCCTCC CAGTGTAGGG CAGGACCTCT CTGGAACTTA CAACCTGCCT 1560
CCCTCAGACA AGGTAGGTTG GAGAATTTCT CTGTGGATGG CTCCTACCCA GGAAGGTAGG 1620
GGAAGGTTAG AGTTATATTT CTAGGTTTTA TGGCTGGCTT TCAGGGAGAG GGGTTCTAGA 1680
TTCTATGACC CACCTTGAGG AAGAATTCTG GTTCCGTTTT TCTTTTATCT TTTTTTTTTT 1740
TTTTTTGTTA AGAGAGATGG GGATTTGCTA TGTTGCCCAG GCTGGCCTCA AACTCCTGGC 1800
CCTAAGTGAT CCTGCTGCCT CGGCCTCCCA GTGTTGGGAT TACAGGCGTG AGCCACTGTG 1860
CCCAGCCGCC TAGTTTCTAT GACTCACTTC AGGGGAGAAG GAGGGTGAGA GAGACAGGAA 1920
GGCAGAAGGA GGTGAGAGAG ACTTTGCTTC TGAGGGCCCC TTCTGAGCCC TTCTAGTCTT 1980
CTTTAGTTCA AGTACGTAGC ATGCCACAGC ACCTTTCTTT GGGGTGTTGT TTTCTGAGCC 2040
CCAACATTCA TGGCCCTGAA TGTGTGCCTC TGTGTGCCAG GTGTTGCCCT AAATTCTTGG 2100
ACCTTCCCAT GAGCTGGAGT TCACTGACCC ATTTGACAGA TGAGGAAACT GAGGCACTGG 2160
GAGAAGCAAA GAGACTTGCC TGGGATCATG AAGTGAAGGG GATCTGAACC CTGAGACAGG 2220
AACTCTTGAT CCCAAGGGGC CCCTAACCCC AAGCCCTTGG CCCCCTGCTG AACTGGTTCA 2280
AACCAGAGAG TGTATAACCC AGCTCCAGGC TGGGCTGGGC CTGAGGTGTG CGTCTCACCT 2340
GGCAGTTACA AGAAAAGGAA ATTGCACTGG TTGCCACATT 2380