EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS087-20119 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr9:93954830-93957060 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs200760632chr993956003hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:93956847-93956865CTCTCCTTCCCTCCCTCC-6.44
EWSR1-FLI1MA0149.1chr9:93956851-93956869CCTTCCCTCCCTCCCTCC-6.94
EWSR1-FLI1MA0149.1chr9:93956855-93956873CCCTCCCTCCCTCCTTCC-7.12
MEF2AMA0052.3chr9:93955577-93955589GCTATTTTTAGC-6.44
MEF2AMA0052.3chr9:93955890-93955902TCTATTTTTAGC-6.92
MEF2AMA0052.3chr9:93954859-93954871TCTATTTTTAGA-7.22
MEF2BMA0660.1chr9:93955890-93955902TCTATTTTTAGC-6.44
MEF2BMA0660.1chr9:93955577-93955589GCTATTTTTAGC-6.92
MEF2CMA0497.1chr9:93954858-93954873GTCTATTTTTAGATC-6.9
NR2C2MA0504.1chr9:93956220-93956235AGGGGTCAGAAGTCA+6.18
TBPMA0108.2chr9:93955273-93955288CTATAAAAAGGCCCC+6.22
ZNF263MA0528.1chr9:93956835-93956856TTCTTTCTCTCTCTCTCCTTC-6.01
ZNF263MA0528.1chr9:93956854-93956875TCCCTCCCTCCCTCCTTCCTC-6.19
ZNF263MA0528.1chr9:93956843-93956864CTCTCTCTCCTTCCCTCCCTC-6.33
ZNF263MA0528.1chr9:93956855-93956876CCCTCCCTCCCTCCTTCCTCT-7.19
ZNF263MA0528.1chr9:93956847-93956868CTCTCCTTCCCTCCCTCCCTC-7.74
ZNF263MA0528.1chr9:93956851-93956872CCTTCCCTCCCTCCCTCCTTC-8.54
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_24346chr9:93955224-93956980Colon_Crypt_2
SE_25080chr9:93954487-93958229Colon_Crypt_3
SE_26319chr9:93953887-93962638Duodenum_Smooth_Muscle
SE_27567chr9:93953700-93957026Esophagus
SE_28201chr9:93953588-93961571Fetal_Intestine
SE_29279chr9:93953698-93962183Fetal_Intestine_Large
SE_32161chr9:93953837-93959264Gastric
SE_35319chr9:93953586-93962988HepG2
SE_39461chr9:93953161-93957016Jurkat
SE_44449chr9:93953709-93961317NHDF-Ad
SE_44911chr9:93953704-93960917NHLF
SE_47822chr9:93954797-93956767Pancreas
SE_51473chr9:93953007-93961399Skeletal_Muscle
SE_52908chr9:93953760-93959405Small_Intestine
SE_65791chr9:93952890-93959470Pancreatic_islets
SE_66540chr9:93953161-93957016Jurkat
SE_67269chr9:93952624-93957244MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr99395524393955725
Number: 1             
IDChromosomeStartEnd
GH09I091191chr99395331293962483
Enhancer Sequence
CTTATTTTTG CAGGTTATGC TCATTCAAGT CTATTTTTAG ATCTTGTTCC TAAATAAGTA 60
CACCAGAATA GCATTCAGTT TGAAAATCAC CATCTGTTCA GAGCAATGAG CTTGGCCTCG 120
CTGGGCTGGG TATACCTGGC CCATGGCAAG GTGGCAGTCC CCTTGTGGAC TGAACCGAGG 180
GGGCAGTTTC AGGTCTCCAA GTGGTGTTTG AAGAATGCAC TAAAAACAGT CACAGGCAGT 240
TGGCATTTTA AATGCCCATT AAACAACTAT TAATATATTT TATTTATAAG CTGAGAACCA 300
CACAAAAAAT GCCCTTGGCT TTTTAAAAAG AAGTTCAAAT AATCCCTTGT ATTTAAATAG 360
ATTTCTTATA AAAAGGCGAT CCAGCCTAAG TTTGGTAGTT AAGATAAAAA TTAACCTATG 420
GAAAAGAAAG CCAGCTCAGA ACGCTATAAA AAGGCCCCTT CCCCCCCCCC CTTTCTTCCG 480
GTGTATGGTG GCCCTCCCCT CCCTCTGCAG CCACTTGGTA GTGACTCACG CTTTTCTTTG 540
GAAATGCAGT TGCTGCGTGA AACACAACGT GAGAATGGGA ATCTGACATA TGAGTAACCC 600
GGCCGAGAGG CACCTCTTGG AAATGACACT GGGCCTTGGC TAGAATTACG CACAGGCCCT 660
GGGAGGGCTG CGGCTCGTAG GCCCGTAGGG GGCAGGGTGA GGGCGGAGGT CCTGGCGCCC 720
CCAGGCCTGA CCCGCCCGCA CCGCTGGGCT ATTTTTAGCG TCCACTAAAC TTAGCCGACT 780
CCACCCTCTT GAATAACCCA CATCTTAAAA TGCTATTTTT CTCCAACAGG TCAAAAGAAT 840
TCTGCGAGTT AGAGCGCAGA TTAAGTTGCT AGCGACGGGC ATTGAAGGTT TTAGAACCGA 900
GAAAATGAGC CGGTGGCGGG GAGCGCGTCC TCAGCGGCCA GGCCCGGCAC GGGGCTCGGG 960
CACTCGGGGA CACACGGTGG TCGTCGCTGT GTCTCAGCAG GACCCTGTGC GCTGGAGAGC 1020
TTGGGGCCGC GAGTCGCGCA GCAAGGAGGC TTCTGGCTTC TCTATTTTTA GCCTCTGAAC 1080
GTTTTCCAAA ATAATTACCA AAAGGAAATA CACACGCACA CATGGACCTA ACACACAAAA 1140
CGTCCTTCTG CGGGAAGCCA GCACTAGGAA AGAAAAAAAA AAAAATCCGA AGTGAAATTA 1200
TGACACAGGG TTTTGTAACC CGCGGTGGCG CGCTTCTGAA ACCCGAGCCC GGCAGCGGCT 1260
TCTTATCTGC ACCGCGTTCC AGGAAGCAGC CGGCGTTTCG GCCGCGCAAG GGCAGCCGCC 1320
GCACGTAGGC AGCGTCCCCC AGCCCGGGAC CCGCAGGAAT GCGAGGGGCA AGACAGATCG 1380
CCGGAGGAGC AGGGGTCAGA AGTCAGTGTT TAACCACTCA CTGGCTTTCG GTGAAGCCAG 1440
AATGTTAGCA GCGAGTCGCG GTCGGGGGCC TTGGGGTTGC ACACGCTTGC TCCAAGCACC 1500
GAGGCTCAGC TGAGCACATG CACAACCCTC TCGATGCAGC GGAAAGTCGT GTGGCTTAGG 1560
GCCGCACCCC GAATTTCGCC GCACCCGCCG CTGTGCCATT TACAACCCCC CACCCCGCCA 1620
CTGCTGTCAC GTAGCAATCA AGAGTAAAGG TTATCACAAA GTCTGTTCTT CGAAGGAAAG 1680
AGTTGGAATC AAGGACTTCG GACGGGAGGA AGTTGGTAAG TTACCGCTTC CTCCCTCCTG 1740
TTTTCCTCTC CTTGTTTAAC TTCTCACAAG AACATGTGGC AGCGCTGCAG GTTAACTCAT 1800
CTTACATAAC TTCGGGGCCG TGTCAACTGT TCAGAAGAAA GAAAAACAAG TATTCTCTTC 1860
TGTAGAAGTT GTATTTAGAA ACAGGCTCTG TTGTTTAGGA CAAGTTCACT TGTGTTGCCT 1920
GATCACTTGC AGCAGAAAAT CTTAGAACTG CTCCTCAAGC AACAAAAAGT AGGGGCTCCC 1980
ATTTCCATCT TTCTTTCTTT TCTTTTTCTT TCTCTCTCTC TCCTTCCCTC CCTCCCTCCT 2040
TCCTCTCTCT CTCTTTCTTT CTTTCTGATG GAGGCTTGCT CTGTCGCCCA GCTGCAGTGC 2100
AGTAGCACGA TCTCAGCTCA CTGCAACCTC CGCCTCCCGG GTTCAAGCGA TTCCCCTGCC 2160
TTAGCCTCCC GAGTAGCTGG GACTACAGGT GCGCACCACC ACGCCCAGCT AATTTTTTGT 2220
ATGTTAGTAG 2230