EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-15140 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr17:71300130-71302470 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr17:71300135-71300146GGTGACTCATT+6.02
Gfi1bMA0483.1chr17:71302371-71302382AAATCTCAGCA+6.32
IRF2MA0051.1chr17:71301567-71301585TGTTTGGTTTCACTTTGC-6.37
ZBTB18MA0698.1chr17:71300737-71300750AATCCAGATGTGC+6.62
ZNF263MA0528.1chr17:71302239-71302260GGTGGAGGTGGGAAAAGAGAA+6
ZNF740MA0753.2chr17:71300792-71300805GTGGGGGGGGCGG-7.82
Znf423MA0116.1chr17:71301630-71301645GCCACCTTGGGGTCT-6.07
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00203chr17:71299491-71309355Adipose_Nuclei
SE_00919chr17:71300026-71303780Adrenal_Gland
SE_01949chr17:71299943-71303692Aorta
SE_02957chr17:71300764-71302343Bladder
SE_04533chr17:71300694-71303709Brain_Anterior_Caudate
SE_06356chr17:71299708-71309411Brain_Hippocampus_Middle
SE_23373chr17:71300486-71302465Colon_Crypt_1
SE_23953chr17:71300656-71302410Colon_Crypt_2
SE_24951chr17:71300591-71302453Colon_Crypt_3
SE_26142chr17:71299583-71309200Duodenum_Smooth_Muscle
SE_26892chr17:71299999-71309123Esophagus
SE_28228chr17:71300129-71302497Fetal_Intestine
SE_29551chr17:71300377-71302695Fetal_Intestine_Large
SE_30277chr17:71300294-71303670Fetal_Muscle
SE_31497chr17:71300428-71303667Gastric
SE_34366chr17:71299962-71309336HCT-116
SE_34727chr17:71299392-71309277HeLa
SE_40779chr17:71299798-71309194Left_Ventricle
SE_41738chr17:71300799-71302044LNCaP
SE_42276chr17:71299727-71303750Lung
SE_44396chr17:71299806-71303677NHDF-Ad
SE_45062chr17:71299792-71302475NHLF
SE_46731chr17:71300839-71302276Ovary
SE_47498chr17:71300524-71302346Pancreas
SE_48667chr17:71300103-71303657Right_Atrium
SE_49576chr17:71300881-71302199Right_Ventricle
SE_50297chr17:71300393-71303675Sigmoid_Colon
SE_52570chr17:71299986-71303669Small_Intestine
SE_53786chr17:71299860-71303700Spleen
SE_54836chr17:71299865-71309532Stomach_Smooth_Muscle
SE_57720chr17:71301035-71301934VACO_503
SE_65340chr17:71300143-71309341Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177130047171302436
Enhancer Sequence
TAAATGGTGA CTCATTATCA AGAACACTCC GGAATAACAT CTCTCCATGT GGATCCCAAC 60
AGATAGCAAG ACTGTGTGCT GAGGAACCCA CTCTAAGGAA ATACTATTCT AGACCCTACC 120
TAACCTCAGG GGTAGACCCC TCCCCAGACT CTGCAGTAAC TATTCCTGGG CCACATGTCA 180
TGGAGAAAAT ACGAGAAAGA ACTAAGATTT GTTGAGCTTT TTACTCTGCA CCAGGCATTG 240
TGTTAGGTGA TTTATTTTGA TTAAACTGTC TCTTTTCTTC TTCTTCTTTT TTTTTTTTTT 300
CCTGAGAGAG GGTCTTGCTT TGTCCCTCAG GCTGGAGTAC ACTGTAGCAG TGCAATCAAA 360
GCTCACCGTA ACCTCAAACT TCTGGGCTCA AGCCATCCTC CTACCTCTGC TTCCCAAAGT 420
GCTGGGACGA TAAACTTTGT AGTCATACAC GGTCCCAAGC ATTTGAAAAA CTTTATCTCA 480
TGTATTCTTC CCAACAATCC CATGGAGTTA TCACTATCAT CCCCAGCTCA CAGATAAGAG 540
CACCGAGACT TAGAGGGGCA CGTGCTCTAC TCAAGTCACA CACGGTTGGT TAGGAGAGAG 600
AGACAAGAAT CCAGATGTGC TGGACTCTGG GTTTTTTCCA CTCCACCATA AGGAACATCG 660
GGGTGGGGGG GGCGGGTGGT GCGAGGGGGA CAGTGCATCA TAAGTGTCCC TGGGGCTCAG 720
GCCTGGGAGG GCTGCTCAAG GCTCTGGATG CATGAGTACA CACAGGATAC GCAGTTGTGC 780
ACACAATTTC AGGTTAACAT CTCCTGAGTC TGAGCACCTC ATTCCCCACC ACTCCAGGGA 840
ACTTATAGAT TAATCCTGGA AAATACAGGC TACAGCCCAA CACCCCAGGT CCATCCAGGG 900
GAGCCTCCTG CTCCTTGTGG GCTGGGAACC AGCTGCCCTG CTTGTCTCCT TCATCTTCGT 960
TCCTGCACCC ACCTCATCCT TATCCTCATC CCCATCCCAG AACCACAGGC TTCAGGCCAG 1020
GGGAGAAGCA GGTCAGCAGG AGGTGAAGGG GAAACCTTCC CTCACCTCCT GGGAATTAGA 1080
ACAGCACAGA GAAGGGAAGA AAAAGGAGCC AAGACTAGGG AGTGACCGGA AGCAACAACG 1140
GAGGAGTCAA GACGAAGAGG AGCCAGTGAC TCAAGGACAT CCGGCAACTT CACTTGATTA 1200
CAGGGCCCTT CCTGGAAATG TGTGCTTCCC GGAGCCACCA CCCGAAGCCA GCCACCAGCA 1260
GAGGGACCAT CTGGGCCAGG CAGGATGGAT GCCTGGTGGG GGGCCCCACT GCCCCCATAC 1320
AGGCTGGGCC CTCCTCCTCT AGGAGTGGTG CTACTACTGG GCAGCAGGGT GCCTCCCTCC 1380
TGCTCGGGAG TGATCGCAGA GGAAAGTGCC GCGCTTGAAA TCAGATCTGC CAGGCCTTGT 1440
TTGGTTTCAC TTTGCCGCTC CTAAGAGCCG GGTGCTCAGC TAAGAACTGG GAATTTCATG 1500
GCCACCTTGG GGTCTCCAGG AGACTGGCAG ATCTAAACTC CCTCCAGAGC AGACAGGCTA 1560
ATCTTGCATC TTGGCCCTGC CGGAAGTTGG GGACAAAGAG CCCCACTCCC TAGGTCACAA 1620
GGTGGCCTGC CACGTGGGTC AAGTTATTTG TGCCTCAGTT TCCTCATTAG CTCTCAGAAC 1680
AATTGATAAC ATTACATAAC TCCCAAGTGC TGTGCTCGGG TGAGCACAGT TCCATGTGTG 1740
CTATAAAGAT GATGCTGTCA CACCCAGTGA CACTCCAGCC ACTGTCACTT CGCAAACTTC 1800
ATAGAGAACA GCCACCTGAG AGCACCTAAT TCAAAAGTCT GTACAGTGAA ACGTGGGCTG 1860
AGACAATGGG TTGACCCTTT TCAAAGTCCT GGGGGTTCCC AGGATTATCT GATGCAGGGG 1920
GAAGGGTCCC CCAAGCTGCT GAAGCCCAGG TACAGATTCT GCCCTCCCTC TGTAGTCTCT 1980
GCCAGCAGTC GGGGGCAGGA AACCCTCGGA TCTGGTTTCT TTCCTGATCT GAGTTCCCTC 2040
ATCCCGTCAC CTTTTAACCT TTAATGATGC CAGAAGAAGG AGCCTGGCTT CTCTCAGACA 2100
AGATGGTGAG GTGGAGGTGG GAAAAGAGAA GCTCCTCCAT TCCTTCCTAG GATAAGGGTA 2160
AAAGTAACTC AGGAATTTGC CAGACCCCGG GTGCTACTAG CAACAAATAA TGCACAGGCC 2220
AGGCACCGTG GCTCATGCCT GAAATCTCAG CACATTGGGA GGCAGAGGCA GAAGCAGGAG 2280
GATCGCTTGA GCCCAGGAGC TTGAGACCAG CCTGGGCAGC ACAGTGAGAC CCTGTCTCTA 2340