EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS146-15074 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr9:93953960-93956920 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs200760632chr993956003hg19
TF binding sites/motifs
Number: 18             
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
MafbMA0117.2chr9:93954777-93954789AAATTGCTGACA+6.37
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: 19             
IDCoordinateTissue/cell
SE_24346chr9:93954308-93954719Colon_Crypt_2
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_47822chr9:93954245-93954760Pancreas
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
GACGGGATGG GCAGCCCCAG GGCCAGCCAT CCCAAGTCTA GGGCTTGCTG GGGCCTAGAC 60
TTTTGACCTC CAAAGGGTAC GGAGTCTGGG GACCACTCTG CACACCATCC TCCATCCAGA 120
GAGAGGGGCC ATTTCCATCC TCATTCGGTT TCCCATATTC AGGGGAACTC CTCTCCAAGA 180
AGAAACAAGG GCTCAGTTCC ATTTCTGACT TCTCTCTAGG TCAGCACGTG CGGTCACTTC 240
ACAGAAAAAT GGTGTGGATG TGCCAGACTG GGGACAAAGG CCCTCTGTTG TCCCCATTAC 300
CTGTGGTTTC CTGCCACAAA GGCTACACCA AGTACCTTAT AAAGAAGGGC TGAGCGCTTC 360
ATGGATTTAC TCAAAACCCA GCGCTCTGGG CTACTATGAC CCCAGCCACC AACAGGTGTT 420
GAGACTCCCC TGAGGCCCCG CCAAAACTGG CTGGGGTTTC CTCTCCACCT CAGTGCCACC 480
CCTGTCTCCA AGCCCATACT CCCAGGCATC TCTCAATCAC TACCTCTACA AGACCCCAGG 540
GTCTGGGTAA TGGGGGCTGG CAGAGCCTGG ACTCATTCCT GCAATGACGT CGGATACCAG 600
CGGCACCCAT TCCCTCTCCA AAGCTCATGT CCACAAGGGC AAACGATAGC ATCCCCCTCC 660
ACCCCGGCAG TAAGCAGCAG CGAGTCTCAC CAATTTGAGA GTCTCTAGAA CAACAGATGG 720
TAATTTGTTG ACACAAAGAT TTAAGGGGAC TCAATTACAG TCCCACTGAA AAAGCTCTCT 780
CTAAAATAAG AAAGTATACA GATTCCTCAG CTCGCAGAAA TTGCTGACAG CTTTGTTTTC 840
AACCCTCCAG GAGTAAAAAG AAGCTGACAA CTTATTTTTG CAGGTTATGC TCATTCAAGT 900
CTATTTTTAG ATCTTGTTCC TAAATAAGTA CACCAGAATA GCATTCAGTT TGAAAATCAC 960
CATCTGTTCA GAGCAATGAG CTTGGCCTCG CTGGGCTGGG TATACCTGGC CCATGGCAAG 1020
GTGGCAGTCC CCTTGTGGAC TGAACCGAGG GGGCAGTTTC AGGTCTCCAA GTGGTGTTTG 1080
AAGAATGCAC TAAAAACAGT CACAGGCAGT TGGCATTTTA AATGCCCATT AAACAACTAT 1140
TAATATATTT TATTTATAAG CTGAGAACCA CACAAAAAAT GCCCTTGGCT TTTTAAAAAG 1200
AAGTTCAAAT AATCCCTTGT ATTTAAATAG ATTTCTTATA AAAAGGCGAT CCAGCCTAAG 1260
TTTGGTAGTT AAGATAAAAA TTAACCTATG GAAAAGAAAG CCAGCTCAGA ACGCTATAAA 1320
AAGGCCCCTT CCCCCCCCCC CTTTCTTCCG GTGTATGGTG GCCCTCCCCT CCCTCTGCAG 1380
CCACTTGGTA GTGACTCACG CTTTTCTTTG GAAATGCAGT TGCTGCGTGA AACACAACGT 1440
GAGAATGGGA ATCTGACATA TGAGTAACCC GGCCGAGAGG CACCTCTTGG AAATGACACT 1500
GGGCCTTGGC TAGAATTACG CACAGGCCCT GGGAGGGCTG CGGCTCGTAG GCCCGTAGGG 1560
GGCAGGGTGA GGGCGGAGGT CCTGGCGCCC CCAGGCCTGA CCCGCCCGCA CCGCTGGGCT 1620
ATTTTTAGCG TCCACTAAAC TTAGCCGACT CCACCCTCTT GAATAACCCA CATCTTAAAA 1680
TGCTATTTTT CTCCAACAGG TCAAAAGAAT TCTGCGAGTT AGAGCGCAGA TTAAGTTGCT 1740
AGCGACGGGC ATTGAAGGTT TTAGAACCGA GAAAATGAGC CGGTGGCGGG GAGCGCGTCC 1800
TCAGCGGCCA GGCCCGGCAC GGGGCTCGGG CACTCGGGGA CACACGGTGG TCGTCGCTGT 1860
GTCTCAGCAG GACCCTGTGC GCTGGAGAGC TTGGGGCCGC GAGTCGCGCA GCAAGGAGGC 1920
TTCTGGCTTC TCTATTTTTA GCCTCTGAAC GTTTTCCAAA ATAATTACCA AAAGGAAATA 1980
CACACGCACA CATGGACCTA ACACACAAAA CGTCCTTCTG CGGGAAGCCA GCACTAGGAA 2040
AGAAAAAAAA AAAAATCCGA AGTGAAATTA TGACACAGGG TTTTGTAACC CGCGGTGGCG 2100
CGCTTCTGAA ACCCGAGCCC GGCAGCGGCT TCTTATCTGC ACCGCGTTCC AGGAAGCAGC 2160
CGGCGTTTCG GCCGCGCAAG GGCAGCCGCC GCACGTAGGC AGCGTCCCCC AGCCCGGGAC 2220
CCGCAGGAAT GCGAGGGGCA AGACAGATCG CCGGAGGAGC AGGGGTCAGA AGTCAGTGTT 2280
TAACCACTCA CTGGCTTTCG GTGAAGCCAG AATGTTAGCA GCGAGTCGCG GTCGGGGGCC 2340
TTGGGGTTGC ACACGCTTGC TCCAAGCACC GAGGCTCAGC TGAGCACATG CACAACCCTC 2400
TCGATGCAGC GGAAAGTCGT GTGGCTTAGG GCCGCACCCC GAATTTCGCC GCACCCGCCG 2460
CTGTGCCATT TACAACCCCC CACCCCGCCA CTGCTGTCAC GTAGCAATCA AGAGTAAAGG 2520
TTATCACAAA GTCTGTTCTT CGAAGGAAAG AGTTGGAATC AAGGACTTCG GACGGGAGGA 2580
AGTTGGTAAG TTACCGCTTC CTCCCTCCTG TTTTCCTCTC CTTGTTTAAC TTCTCACAAG 2640
AACATGTGGC AGCGCTGCAG GTTAACTCAT CTTACATAAC TTCGGGGCCG TGTCAACTGT 2700
TCAGAAGAAA GAAAAACAAG TATTCTCTTC TGTAGAAGTT GTATTTAGAA ACAGGCTCTG 2760
TTGTTTAGGA CAAGTTCACT TGTGTTGCCT GATCACTTGC AGCAGAAAAT CTTAGAACTG 2820
CTCCTCAAGC AACAAAAAGT AGGGGCTCCC ATTTCCATCT TTCTTTCTTT TCTTTTTCTT 2880
TCTCTCTCTC TCCTTCCCTC CCTCCCTCCT TCCTCTCTCT CTCTTTCTTT CTTTCTGATG 2940
GAGGCTTGCT CTGTCGCCCA 2960