EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS020-46057 
Organism
Homo sapiens 
Tissue/cell
CD34+ 
Coordinate
chr9:132113320-132115600 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73621547chr9132113931hg19
TF binding sites/motifs
Number: 30             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CrxMA0467.1chr9:132113867-132113878GAGAGGATTAG+6.02
KLF16MA0741.1chr9:132114584-132114595GCCCCGCCCCC+6.02
KLF5MA0599.1chr9:132114573-132114583GCCCCGCCCC+6.02
KLF5MA0599.1chr9:132114584-132114594GCCCCGCCCC+6.02
KLF5MA0599.1chr9:132114549-132114559GGGGCGGGGC-6.02
SP2MA0516.2chr9:132114580-132114597CCCTGCCCCGCCCCCTC+6
ZNF263MA0528.1chr9:132113794-132113815GAGGGCGGAAGAGGAAGGGAA+6.04
ZNF263MA0528.1chr9:132113695-132113716GGGGAAGCAGGAGGAGGAAAG+6.22
ZNF263MA0528.1chr9:132113920-132113941GGTGGAGGGGGTGAGGAAAGG+6.27
ZNF263MA0528.1chr9:132113708-132113729GAGGAAAGGGGGGGAGGGGGA+6.28
ZNF263MA0528.1chr9:132113762-132113783GGAGGAAAAGGAAGGGGGAAG+6.4
ZNF263MA0528.1chr9:132113775-132113796GGGGGAAGAGGGGGCAGAAGA+6.54
ZNF263MA0528.1chr9:132113956-132113977TGGGGAGGAAGATGAGGGGAG+6.57
ZNF263MA0528.1chr9:132113848-132113869AGGGGAGAAGGGGCAGGAGGA+6.69
ZNF263MA0528.1chr9:132113717-132113738GGGGGAGGGGGATGGGAGAGG+6.81
ZNF263MA0528.1chr9:132113750-132113771GATGGAGAAGGGGGAGGAAAA+6.81
ZNF263MA0528.1chr9:132113707-132113728GGAGGAAAGGGGGGGAGGGGG+6.86
ZNF263MA0528.1chr9:132113800-132113821GGAAGAGGAAGGGAAGAGGGG+6.86
ZNF263MA0528.1chr9:132113851-132113872GGAGAAGGGGCAGGAGGAGAG+6.95
ZNF263MA0528.1chr9:132113778-132113799GGAAGAGGGGGCAGAAGAGGG+6
ZNF263MA0528.1chr9:132114199-132114220TTCCCCTCCCCGCCTTCCTTC-7.05
ZNF263MA0528.1chr9:132113950-132113971GGAGGATGGGGAGGAAGATGA+7.23
ZNF263MA0528.1chr9:132113678-132113699TGGGGAGGGGGAGGAGAGGGG+7.26
ZNF263MA0528.1chr9:132113698-132113719GAAGCAGGAGGAGGAAAGGGG+7.27
ZNF263MA0528.1chr9:132113944-132113965AGGGGAGGAGGATGGGGAGGA+7.48
ZNF263MA0528.1chr9:132113753-132113774GGAGAAGGGGGAGGAAAAGGA+7.52
ZNF263MA0528.1chr9:132113746-132113767GGAGGATGGAGAAGGGGGAGG+7.59
ZNF263MA0528.1chr9:132113759-132113780GGGGGAGGAAAAGGAAGGGGG+8.06
ZNF263MA0528.1chr9:132113704-132113725GGAGGAGGAAAGGGGGGGAGG+8.97
ZNF263MA0528.1chr9:132113947-132113968GGAGGAGGATGGGGAGGAAGA+9.76
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_04701chr9:132113139-132114634Brain_Anterior_Caudate
SE_06449chr9:132114142-132116676Brain_Hippocampus_Middle
SE_08526chr9:132114467-132116027Brain_Inferior_Temporal_Lobe
SE_09390chr9:132112910-132115292CD14
SE_27074chr9:132112820-132116466Esophagus
SE_29978chr9:132113093-132116939Fetal_Muscle
SE_31911chr9:132112881-132113916Gastric
SE_31911chr9:132113968-132116545Gastric
SE_34442chr9:132114713-132116299HCT-116
SE_42813chr9:132114661-132116526Lung
SE_54065chr9:132114061-132114722Spleen
SE_54065chr9:132114968-132115860Spleen
SE_65687chr9:132113402-132116095Pancreatic_islets
SE_68873chr9:132112292-132116082H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9132113536132114600
Number: 1             
IDChromosomeStartEnd
GH09I129350chr9132112561132116979
Enhancer Sequence
GGAAACCGAG ACTCAGCCAG CTGAGGGGCT AGTCCAGGCC CCCTAGGAAG CCGAGGTGGC 60
CTCAGCCTCC AGGCCAGGGC TTCCTAGGAC TGCAGTCCTC TCCTGCCCCT CTTCAGCCCC 120
GCCTTCCCCG CAACCCCAGC ATCCCCTGTC CTCTGGAGGA AGATTTCCGT GGTCCCGGTT 180
GGGGGTGCCA AACTGCCAGC GACAACAGCG TTTTTTAAAT CCTAGAGTCG CTGACTCGTG 240
TGATTATTCT TATTTAAGGC AGGGAAGGTA CTGGGAGTGG GGAGCCGGTC ACCTCTGGGT 300
GGGGGGCACC TCCGGGTGAG GGCGGCCCCT CCTGTCTGCC TTGTGCCCAG CTCCAACCTG 360
GGGAGGGGGA GGAGAGGGGA AGCAGGAGGA GGAAAGGGGG GGAGGGGGAT GGGAGAGGAT 420
GAATTAGGAG GATGGAGAAG GGGGAGGAAA AGGAAGGGGG AAGAGGGGGC AGAAGAGGGC 480
GGAAGAGGAA GGGAAGAGGG GGCTGGGGTA AGGGGAGAAG AGGGTAGGAG GGGAGAAGGG 540
GCAGGAGGAG AGGATTAGGG AGGGAGATGA GAGGGGAAGA GGAGGCTAGG GAGGGCGTGG 600
GGTGGAGGGG GTGAGGAAAG GGCTAGGGGA GGAGGATGGG GAGGAAGATG AGGGGAGCAC 660
AGAAAAGAAC CCCCCCGCCC CCGCCTTGGT GGCTCCCTAA GCAGATAGGA GATACATAAT 720
TTACTACGGA AATGCAAAAA GAATTGGGAA ACTCTCAATT TATAAATATT TATTTTTACA 780
AGTTCGCCCC TCCCGGCTCC CCCTTGCTGG CCCTGGTCTT TTCTCTCTGG GGCCCTCGGG 840
GCGCAGGTCC CTCCTCTCCG GCTCCCACTC TGGCCCCTCT TCCCCTCCCC GCCTTCCTTC 900
TGCAGTCCCT TCCCCCTCGG GCGGTCTCTG TCTCCCCCAG GTCCTCTCCT TCCTCTCTCC 960
CGCCTGTGTC TCTCCCCCTA GTGCGTCTCT GTCTCTGTCT CTCTTTGTGG CGGGACGGGG 1020
GCGATTTTTG AGTCTCCCCC GCCGTGGGTT TCTGTCTCTC TGGCTGTCTC CCCCATCTCT 1080
CCATCTGCGT CCTCCCACTT GCCCCGCGCC CCCCGTCTCT CACACCCGAG GACCCCAGCT 1140
CCCGCCAGAG GGTCCGGGGG CGGCAAGAGC CCCCGTAGGC TCCCGGGGGA TGGGGGGAGG 1200
GGTCGTTTCC CTGGCAACAG CCGGTCGGCG GGGCGGGGCG GGAATTGGGT TGAGCCCCGC 1260
CCCTGCCCCG CCCCCTCGCC CTGGCCGCGG GTTGGGGGCG CCTGGGTGAG GCTTCCGAAG 1320
CACGTGGACC GGGCCGTGGG GGCGGGAGGG GGCTCCCTGG GAGGCCGGCC CGGAGGAGGG 1380
GCGGGCAGGT AATCAGCCAA TCAGTTAATC AATCGGCGGG TCAATCCATC AATCACAGGC 1440
CCCCAGAGCG GCTGGGGTTG AGCGCTCAGG GTGTGGAAAG AGCTGAGTTC TAATCCCTGC 1500
TCGGCCTCTT CCTGGCCGTG TGGCCCCCAA GCCCGGAAGC CCCTGCACAG CGCCGAGCCT 1560
CGGGGTCCCC TCTGCGCAGT GGGGCTGTGG CAGCACCTGC CTGCGGGGCT GACAGTCCTT 1620
CCTGGTGGCC TGGTAGTCCC TGTCCACCCC TCCACCTCAC GGATGGGAAA CGGGAGCTGC 1680
TGAGAGGGGA AGTGGCCGGT GGGCACAGAA GGGATGGAGC GGGGAGGGGC ACCAGCCATT 1740
TCACAAGCTC GGCTGCATCT GCTGGCCCAG GCCGTTTTTT TTTTGTGAGC GGGGCCTGCG 1800
CTGTCCCCAT CCTTGGCAGC ACCTAGCTCA GTGCCCGACC TGCACAGGTC CTGGCTTCAG 1860
GTGGGAGAAC CCGAAATGCC CTTTTGATCG CTCCTCCCGG TCCCTCTCCC CTCCTGGGGT 1920
GGGGAACTGA GTCCGGGAGA GGCCAGATGG ATGCAGGGTT GCTTGGCTAG ACCCGTGCCG 1980
GCCCCTCCTC TTAAGCCATC CCTAGGCCTG ACACATGAGC TGGGGTGGGG CGGTTGTTTG 2040
TTAGTGAAGG AGGAGGCCTC AGGCAGCGTC TGCAGGGTCA GCAGCTGGAA GGGTCTCTAG 2100
ATGCTTCCTG CAACTCAAAG CCAGTTGTTT GTAACCAACA CGCAGGTCTG CTCAGCCTTC 2160
TAACCAGCAC CTCTCCCAGC CCTGTCCCTC CCTCCCTCCC AAGCGGGCTG GGGGCTGGAG 2220
TGGAGGCTGA TGAAGGGGCT GGTGGGAGGG CCCTCTCCAG GAGGGACTGG GGAGTCACAG 2280