EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS039-00911 
Organism
Homo sapiens 
Tissue/cell
ESC_NPC 
Coordinate
chr10:31421740-31424580 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1776631chr1031422577hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB3MA0638.1chr10:31422761-31422775GCGCCACGTCACCC+6.07
EWSR1-FLI1MA0149.1chr10:31421974-31421992ACATCCTCCCTCCCTTCC-6.3
EWSR1-FLI1MA0149.1chr10:31422196-31422214GGAAAGGAGGAAGGGAGG+6.88
EWSR1-FLI1MA0149.1chr10:31421982-31422000CCTCCCTTCCTCCCTCCC-6.88
EWSR1-FLI1MA0149.1chr10:31421978-31421996CCTCCCTCCCTTCCTCCC-6.92
EWSR1-FLI1MA0149.1chr10:31422192-31422210GAAAGGAAAGGAGGAAGG+7.05
EWSR1-FLI1MA0149.1chr10:31422204-31422222GGAAGGGAGGGAGGGAGG+7.08
LMX1BMA0703.2chr10:31423921-31423932AATTTAATTAA+6.32
MEOX2MA0706.1chr10:31422236-31422246AGTAATTAAC+6.02
Nr2f6(var.2)MA0728.1chr10:31424180-31424195AAGTTCAAAAGTTCA+6.19
Nr2f6MA0677.1chr10:31423949-31423963CAGGTCAAAGGTCC+6.05
RARAMA0729.1chr10:31424180-31424198AAGTTCAAAAGTTCATAT+6.18
RxraMA0512.2chr10:31424173-31424187AAGGTTAAAGTTCA+6.18
ZNF263MA0528.1chr10:31421974-31421995ACATCCTCCCTCCCTTCCTCC-6.09
ZNF263MA0528.1chr10:31422888-31422909CCCCTCCTCGCCCCCTCCCCC-6.36
ZNF263MA0528.1chr10:31422202-31422223GAGGAAGGGAGGGAGGGAGGA+6.63
ZNF263MA0528.1chr10:31421981-31422002CCCTCCCTTCCTCCCTCCCCA-6.85
ZNF263MA0528.1chr10:31422210-31422231GAGGGAGGGAGGAAAAGAGGG+7.25
ZNF263MA0528.1chr10:31422201-31422222GGAGGAAGGGAGGGAGGGAGG+7.9
ZNF263MA0528.1chr10:31422198-31422219AAAGGAGGAAGGGAGGGAGGG+8.12
ZNF263MA0528.1chr10:31421977-31421998TCCTCCCTCCCTTCCTCCCTC-8.35
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_25423chr10:31420765-31433717DND41
SE_30759chr10:31421649-31424498Fetal_Muscle
SE_39587chr10:31421494-31430224Jurkat
SE_66545chr10:31421494-31430224Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr103142360031424302
Number: 1             
IDChromosomeStartEnd
GH10I031132chr103142154631427344
Enhancer Sequence
TGAATTTTGC CCGGTTGTAC ATTTGATGAG TATTACAAAA GAGAAGATGA AAGAGCTACA 60
GGATCCTGTA ACTGGAGGAC CTGATCTGGC CCAGGCACCA GGGAAGTGAC ATTTCACCTG 120
AGGCCAGAGG AATAAGTGGG AGGGGAATGG GCTGGGGGTG GGCTATGCAG GGAGACCTAT 180
GTGGGCAAAG GGCCTTTCTC CTGGTAAGTT TCTACTCACC CAGCCTCCAC CTGGACATCC 240
TCCCTCCCTT CCTCCCTCCC CAGGAGCTGG GCTGAGGGCC GCCCTACTGC TATCCATGGC 300
ACTTGTCACC CAGAGCCCTG GTGAACTGTT TGCTTGTATG CAGCACCCCT CACCACATGA 360
AGAGCATCTC AAGGGCTAGG AGTCTCGTTT CTTGTATCCC TGGTCCACCG CCTGATCTCC 420
AGCACACATG AGGTATCCAT CAAAATGTTA GCGAAAGGAA AGGAGGAAGG GAGGGAGGGA 480
GGAAAAGAGG GAACAAAGTA ATTAACGAAT CCCTAGCTGC AGGCACAGGT TGATTCTCTG 540
CAATGTCTCC TTTTCTGTCA CAGAGAAAAA GAGCACAGTT AGAGTTCACA GGGACCGCGC 600
CCTGCCACAC ATTAATTTAT TCTCCAAACA TTTGTGGAAG TTGCTAGAGA CACAGATGCA 660
ACGTGTTTTC AGGGAGCTTA TGATCTAGCA GTGGAAGCGC AACAGAAGTG CAATTCTTTC 720
ATCCTTTTGC CCACATAAAG CAGGCAAGGC ACGACGAATT TTGATGTCAA CTGCCCAGGC 780
AGGACTTTGT CCCAGCCCAG CGACCCTCAC GAGGCCAAGG GCAGAGATGA TAGTTGTAAT 840
ATACTCTTCT GTCCATTTCC TTGATATTCT CCTCAAGGGG TGGGGGGCGC CTGAAATCCA 900
TCTGCCCCGG GGAGAAGGGC CTCGTGGGCC AGCGCAGCTT GCTCCTCTGC AGACCCAGAA 960
GCATTTGTGC GTCCCGGGCG TGGCAGGCCC GGCGCCCACT CCGCCCTCCC GCCCCTCCCC 1020
CGCGCCACGT CACCCGGGTC ACGTGAGTGA CCAGGCTCCT CACCCCAACC CCCCTCCCTA 1080
CTCCCGCCAG ACTCAGCTGC TCTCCCCGGG AGCTGGGGAG CCGGGGGCGG GCAGCCGCGT 1140
CTGTCCTGCC CCTCCTCGCC CCCTCCCCCG CAGCCTGAGG AGGGCGTTAA GCAAGGGGCT 1200
TCGGAGAAAT TAGAACCAGC GTTCTAAATT AAGGGGAGCA GATGTCCTTG TTTTGCTCGC 1260
GAGGCCTGGG TGGCCTGCTG TTCAGACAGA AATCGTTGAG GCGCTGACCT TCCGGGACTG 1320
CTGTCAATCT CCGCGTGCAG ATGGCCAGCC CGGAGCCTCG CCGCTCCCCT GCATTGGAAA 1380
TGCGGCAGCC GGGGGTGCCG GCAGCTTGAG AGAAAAGTCT GCGTGGAGGG GGGGTGGGGG 1440
GGATGAGGGG AGGCCCGGGG AGACAGAGGG CAGGAGAAAA AGGCCGGCCC CGCTCACAAT 1500
GGAGCCCCTG TGGCGGCCCC TCCGAGACAA TGCGGTCCCC CGGGACCCGC GGTGGGTTGC 1560
GCCAGGCCAG TCCGCGCTCC AGCTGCCTCT TCAGAACAAG GCAGTGCAAA TGTGCCCACT 1620
TGATTCTAAA TCCTCTTAGG CGCTGTCCAT GTGAACAAGG AAAGGGGTGG CCCTACGATC 1680
CTTTACAATC GGAGGCCTGG GGAGGCCTGG GAGCCCTGGA GCTCCGGAAA ATGTCTGCAC 1740
CACGCATGCA AATGGGTCAT TTCGCTTGGA GAGAGGCATC TGGCGACATC GGCAGAAAGG 1800
CTCTCTGCCC GGTAGACGGT GAACAAAACC CACAAAACCA GCCAGCCAAC AGCGTGCACT 1860
AAACACCCCT CTCTGGCCCT TCAATGCCAC CCGGAGTCCT GAAACATTTT CAGGTTGTTT 1920
CCCCTGGAGA GACGTCCCAT GAAATGTTCA GAAAAGCCAG CTGAGCTGTG CAAAGTCATT 1980
AGTCACCCAG GTATTTACAC TGTTTTTCCT ATTTCCTTTC TCTTTTGGCC TCTGTGGTCA 2040
GTGGTATAAA ATTCCTAGGA ACTCCCACCT AAACACCAGC TTCCTGTTTA TTCTTGCAGT 2100
GGCTTTAATG TTTCGCTGTT AAAAGCGGTT GACCAAGACA CTGAAACAAT CAGTAGAGGT 2160
TCGCAGGTGA ATGGAAAAAA AAATTTAATT AAAAAATATA TCTACTGCTC AGGTCAAAGG 2220
TCCAGGTTCA TTTTTACTGC TTATGTCAGA ATCGCAAAGG GGAAAAGGTA AAATTAAAAT 2280
GTAACTTAAT GCCTAAGATC TTGGTTCAGT TTCATTTGGC CCCTGTGTCT ACATGAACCT 2340
ATAAAATACG ATACACTAAA GTATGAATGT TTTCATTTCT AGCAGTGGAA GGCCTTTTTT 2400
TTTTCAATGT GGCATGACGT TCTTTTGTTA GAGAAGGTTA AAGTTCAAAA GTTCATATAT 2460
TAGCACAATC TGTGTGCTCC TGCGTGTGCC TTACACCTCG CTATGCCTGT TCCGCCTTAA 2520
TTTCCTGCAG CAAAACCTTG CATTTACAGA GCCATCAGAA TTGCAGCCTC CCTGGCCTGG 2580
AAAAGAACCC TCGAAGTCAC CTCATTCAAC CCTTTTCCAA TACTGAATTC CCTGTATGGC 2640
CCCTAGGGAG TGTTAGTGAT GGGACCCTTT CTACCTCAGA TTTTATAAAT TTATTTTTTA 2700
GAGACAAGGA TCCACTCTCT CGCCCAGGCT GGAGTGCAGT AGTACCATCA CAGCTCACTG 2760
CAGTCTCTAA CTCCTGGGCT CAAGTGGATC CTCCCACCTC AGCCTATGAG TAGCTGGGAC 2820
TACAGGCATG TGCCACCATA 2840