EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS150-11288 
Organism
Homo sapiens 
Tissue/cell
NT2-D1 
Coordinate
chr9:92049880-92052520 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gfi1bMA0483.1chr9:92050916-92050927AAATCACAGCC+6.02
KLF4MA0039.3chr9:92051645-92051656GGAGGGTGTGG-6.32
Klf1MA0493.1chr9:92050580-92050591AGCCACACCCA+6.14
POU2F2MA0507.1chr9:92050149-92050162ACATGCAAATGAT-6.1
RREB1MA0073.1chr9:92052405-92052425CCCCCACCCAGCACCAACCC+6.66
SP3MA0746.2chr9:92050697-92050710GGCCACGCCCACA+6.64
SP8MA0747.1chr9:92050698-92050710GCCACGCCCACA+6.22
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_03177chr9:92048344-92053491Brain_Angular_Gyrus
SE_03905chr9:92046545-92053775Brain_Anterior_Caudate
SE_04779chr9:92038176-92053883Brain_Cingulate_Gyrus
SE_05782chr9:92038008-92053861Brain_Hippocampus_Middle
SE_06723chr9:92046697-92053775Brain_Hippocampus_Middle_150
SE_07735chr9:92046339-92053618Brain_Inferior_Temporal_Lobe
SE_09037chr9:92051127-92051402Brain_Mid_Frontal_Lobe
SE_09037chr9:92051844-92052149Brain_Mid_Frontal_Lobe
SE_09170chr9:92050137-92051624CD14
SE_09170chr9:92052077-92053725CD14
SE_11886chr9:92051227-92053330CD3
SE_14475chr9:92049153-92050699CD4_Memory_Primary_7pool
SE_14475chr9:92051443-92053297CD4_Memory_Primary_7pool
SE_16354chr9:92051528-92053432CD4_Naive_Primary_8pool
SE_16924chr9:92052250-92053193CD4p_CD225int_CD127p_Tmem
SE_17355chr9:92032066-92053749CD4p_CD25-_CD45RAp_Naive
SE_17792chr9:92047985-92053851CD4p_CD25-_CD45ROp_Memory
SE_18250chr9:92048668-92053803CD4p_CD25-_Il17-_PMAstim_Th
SE_19118chr9:92048956-92051527CD4p_CD25-_Il17p_PMAstim_Th17
SE_19118chr9:92051964-92053297CD4p_CD25-_Il17p_PMAstim_Th17
SE_20089chr9:92050886-92053432CD56
SE_21155chr9:92051412-92053610CD8_Memory_7pool
SE_21665chr9:92051772-92053329CD8_Naive_7pool
SE_21969chr9:92051498-92053290CD8_Naive_8pool
SE_22409chr9:92049770-92053658CD8_primiary
SE_26933chr9:92049392-92053607Esophagus
SE_32149chr9:92049473-92053449Gastric
SE_33121chr9:92048376-92052618H1
SE_41833chr9:92049918-92052874LNCaP
SE_50088chr9:92050024-92053515Sigmoid_Colon
SE_52548chr9:92050161-92053181Small_Intestine
SE_60002chr9:92014899-92064443Ly4
SE_62222chr9:92014516-92154755Tonsil
SE_68703chr9:92047240-92053642H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr99205109192051724
chr99204999992050865
Number: 1             
IDChromosomeStartEnd
GH09I089433chr99204865192053272
Enhancer Sequence
ATTTTTAGGT GAAGCCTTTG AATGCTGCAA CATAATTAAT CCATATATTT TTAATACTGG 60
GAAGTCCCAA CCAAACACAT CTGAGGGCTG AGTTGCTGGT CTAAGAGCTC AGAGTCTACC 120
TGGGCATGGG GGAAGGGGCC GGCCAAGGCG GGGAGTGCAC GGGGGCTGCA CATCCCCCAG 180
GGCATGTGGA GGACAGAAAT CCCCACTAAG AGAGTCATGA TAAAGGCAGT CATAAGGTAA 240
TATTAATTTT AAGAATGCTG GTTGAGTAAA CATGCAAATG ATCATTAACA GGACCTGGAA 300
AATAACCAGA AAACCAGTAC ATTCCATGGG AATCTTGACT TGATGAGCCA TTCAGATGCA 360
AATTTTACCC CAATTCTGGA AGGATTACAA GCATCCCCAT TCACAGCCCC CATTCCTATG 420
TAAATTCTAG TCCGAGGACT GGCCCTCCAG TTCCCAGCCT TCTGGCTGCT TTGCCCTGTT 480
TCTTTCCTTT AGGCTCCTAA GCAAGAGCTG TGGAGTTTCT GGTTTGTTTC TGGCCCCTCC 540
TCCTTTCCCC AACTCACAGA GATGGCAGAC TCCCAGGGCT CTCTGACTTT CACACACCTG 600
GACCATACTA GACACAGTGC CGGGCATGTA CTTTGATTTA CAGAACCCAG GGACAAACAA 660
GGCCACCCAG GTCTCTGTGT CAGCAAAGAT CCTGAACATC AGCCACACCC ACGGCTTTAT 720
GCAGAGCAAG TCCTACAGGC TCCACCTACG CCCCACCCGG CCCCGACCAG CCTGCTGCCT 780
GCTCCTGGAC AACCTGGTCT GGGTGCACCC CTCCCAGGGC CACGCCCACA GGTTGCATGT 840
CCGGCCTTTC CTTACAAAGG CTGTGCAAAA CAGAGAAACT TCGAGATAAA TGAAACTTAA 900
ATAAAGGAAG GGCATGAACA CTGCCCAGTG TCCATATCTG CTGTGCCGCA TCCCAATGCA 960
TGCTGAATTG GCTGCCCAGT AAGAGAAAGC AGGGATAGCC TAGGCCAAGG AAGCGCCCCC 1020
GCTGCCCCCC ACCCCCAAAT CACAGCCTCA GCCTTGGCTG CTCTCTGGCC AGCTACAGAA 1080
TGACGGACAT CTCAGACAAC ATCCTGCACT TCTGTTGTCT TCAAAGCACA GAAGTGCAAA 1140
GCTCTGGAGT GAAGCCTGTA AGGTCCACTC AAGTGTGTTT TTCCTCTGGT TGTCCAGAAG 1200
GGCAGCTGGT CATTTGGTCC CCTCACATTA GAAGGAAGCC CACTTACTCA GCTCATTCTC 1260
ACTCAACCCC AGTGAGGGGT GAGAAATGGG AACACAAGAC CATTTACCAA ATGACAAAGA 1320
AAACCCAAGC CCCTGACCCT GCCCAGCTGG CCTCACCTTT CCAGGGGCCA TGCTCCTGAC 1380
CCCACGCTGG TCAGCGTGTC CTCAGCCACC AGGGAGGATG GATACTCAGG ACACCATCTG 1440
GCCCCGCCGC CCCATCCTCA CGCAGGGCCT CTGCTCGCCT GGGACGTCTG TCCTGACTGC 1500
AGGGGTTTCA AGGGCTCTGT TATTAGTTGG GGCTCAGGCC AGGACTGCTC CAGCCACAAC 1560
AAGGCACCCT TCAGCGCAGG GACAAGGTCC CGTGGTGAGC CTTCTCCGCA GGCTGTGGAA 1620
CAACCCTGTC CCATTCTCTT CCTTTTAAAC AGCGGGGCTG TTCAGCGATG TGGGCCTGAT 1680
TGTTTTCCTG TGTGGGCTAA TTCAGGGGCT CGTGGGGCAG GGCCCAGTCC CAAGGCTGAG 1740
GAAGGAGGAG AAAGGCTGCC TTAGAGGAGG GTGTGGGGGG TTGCGGCCCA GCACCCAAGC 1800
CATGCACACC ATTGTCCACC CATGGAGCAG CAGGTCGCCT GGCGAGGGCA AGCTCCTGGG 1860
TGCCTGAGGA CCCTGCAGGC CTGGCCACTA CTTCAGTCAT CTGGGGGCTC CATGGCAGGA 1920
TGGGTGAGCT GCCTAAGGCC ACGGGACAAT GGGGCTAGAG GTGAAGTCCC GAGGAAGCAG 1980
ATGTAGCCCT GGGCAAGTCA CTCTGGCCCT CTGAGCTCTC ATGTCCAGCC TTGGACTCAG 2040
GAATCACGAA GACAGCTCAG TCAAGAGGTA GCAATGAGGG CAAACTTGGG AGGTGAGCAT 2100
GCACAGAGCT GCTGGACAGT GCTGCAGCGA GATGGCCTGC TCCCAGCTGG GCAGACGACC 2160
CTAAAACAGG AAGCACGTGG CCTCTTTTGT TAGGGGCTGC AGGGCCCTGG CTGCTCTGCG 2220
GGCCAGCATG CCCACCCCCA TGAGTGGCCT GATCCTAGTG GGCATTGCAC AGTGCAATGA 2280
AGTGTGGCTC GTGCAGCTCT GGCAGTTTTT ATTTTTCTGC AGGCCAGGTT TTCCTCCCAC 2340
AGCGGCAGGC ACCTGCCCTC AGCCTGTAAG GAAGCGCGAT GCAGTGAGTA TTGCCCAATC 2400
TTGGTCGCCC ACACTTGGTC TTGAATAAGC AAACAACCAC AGGACAAGCA GCAGGGCAGG 2460
TGTGAAGCTC GCCCTGAGTC TCTGACACTG CAGGTGTGGC CTCCAGATCC CAGCCTCTGC 2520
ACCCACCCCC ACCCAGCACC AACCCTAGCA GGCGGCAGCG ACAGGCACTC CCACTGCTGC 2580
GGTGCGCCCT GAGAGGGGAG GGCACAGGCC TGGCGCATGA CTGGGCTCAG TGACACGGGC 2640