EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-34352 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr9:93953980-93957180 
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
GGCCAGCCAT CCCAAGTCTA GGGCTTGCTG GGGCCTAGAC TTTTGACCTC CAAAGGGTAC 60
GGAGTCTGGG GACCACTCTG CACACCATCC TCCATCCAGA GAGAGGGGCC ATTTCCATCC 120
TCATTCGGTT TCCCATATTC AGGGGAACTC CTCTCCAAGA AGAAACAAGG GCTCAGTTCC 180
ATTTCTGACT TCTCTCTAGG TCAGCACGTG CGGTCACTTC ACAGAAAAAT GGTGTGGATG 240
TGCCAGACTG GGGACAAAGG CCCTCTGTTG TCCCCATTAC CTGTGGTTTC CTGCCACAAA 300
GGCTACACCA AGTACCTTAT AAAGAAGGGC TGAGCGCTTC ATGGATTTAC TCAAAACCCA 360
GCGCTCTGGG CTACTATGAC CCCAGCCACC AACAGGTGTT GAGACTCCCC TGAGGCCCCG 420
CCAAAACTGG CTGGGGTTTC CTCTCCACCT CAGTGCCACC CCTGTCTCCA AGCCCATACT 480
CCCAGGCATC TCTCAATCAC TACCTCTACA AGACCCCAGG GTCTGGGTAA TGGGGGCTGG 540
CAGAGCCTGG ACTCATTCCT GCAATGACGT CGGATACCAG CGGCACCCAT TCCCTCTCCA 600
AAGCTCATGT CCACAAGGGC AAACGATAGC ATCCCCCTCC ACCCCGGCAG TAAGCAGCAG 660
CGAGTCTCAC CAATTTGAGA GTCTCTAGAA CAACAGATGG TAATTTGTTG ACACAAAGAT 720
TTAAGGGGAC TCAATTACAG TCCCACTGAA AAAGCTCTCT CTAAAATAAG AAAGTATACA 780
GATTCCTCAG CTCGCAGAAA TTGCTGACAG CTTTGTTTTC AACCCTCCAG GAGTAAAAAG 840
AAGCTGACAA CTTATTTTTG CAGGTTATGC TCATTCAAGT CTATTTTTAG ATCTTGTTCC 900
TAAATAAGTA CACCAGAATA GCATTCAGTT TGAAAATCAC CATCTGTTCA GAGCAATGAG 960
CTTGGCCTCG CTGGGCTGGG TATACCTGGC CCATGGCAAG GTGGCAGTCC CCTTGTGGAC 1020
TGAACCGAGG GGGCAGTTTC AGGTCTCCAA GTGGTGTTTG AAGAATGCAC TAAAAACAGT 1080
CACAGGCAGT TGGCATTTTA AATGCCCATT AAACAACTAT TAATATATTT TATTTATAAG 1140
CTGAGAACCA CACAAAAAAT GCCCTTGGCT TTTTAAAAAG AAGTTCAAAT AATCCCTTGT 1200
ATTTAAATAG ATTTCTTATA AAAAGGCGAT CCAGCCTAAG TTTGGTAGTT AAGATAAAAA 1260
TTAACCTATG GAAAAGAAAG CCAGCTCAGA ACGCTATAAA AAGGCCCCTT CCCCCCCCCC 1320
CTTTCTTCCG GTGTATGGTG GCCCTCCCCT CCCTCTGCAG CCACTTGGTA GTGACTCACG 1380
CTTTTCTTTG GAAATGCAGT TGCTGCGTGA AACACAACGT GAGAATGGGA ATCTGACATA 1440
TGAGTAACCC GGCCGAGAGG CACCTCTTGG AAATGACACT GGGCCTTGGC TAGAATTACG 1500
CACAGGCCCT GGGAGGGCTG CGGCTCGTAG GCCCGTAGGG GGCAGGGTGA GGGCGGAGGT 1560
CCTGGCGCCC CCAGGCCTGA CCCGCCCGCA CCGCTGGGCT ATTTTTAGCG TCCACTAAAC 1620
TTAGCCGACT CCACCCTCTT GAATAACCCA CATCTTAAAA TGCTATTTTT CTCCAACAGG 1680
TCAAAAGAAT TCTGCGAGTT AGAGCGCAGA TTAAGTTGCT AGCGACGGGC ATTGAAGGTT 1740
TTAGAACCGA GAAAATGAGC CGGTGGCGGG GAGCGCGTCC TCAGCGGCCA GGCCCGGCAC 1800
GGGGCTCGGG CACTCGGGGA CACACGGTGG TCGTCGCTGT GTCTCAGCAG GACCCTGTGC 1860
GCTGGAGAGC TTGGGGCCGC GAGTCGCGCA GCAAGGAGGC TTCTGGCTTC TCTATTTTTA 1920
GCCTCTGAAC GTTTTCCAAA ATAATTACCA AAAGGAAATA CACACGCACA CATGGACCTA 1980
ACACACAAAA CGTCCTTCTG CGGGAAGCCA GCACTAGGAA AGAAAAAAAA AAAAATCCGA 2040
AGTGAAATTA TGACACAGGG TTTTGTAACC CGCGGTGGCG CGCTTCTGAA ACCCGAGCCC 2100
GGCAGCGGCT TCTTATCTGC ACCGCGTTCC AGGAAGCAGC CGGCGTTTCG GCCGCGCAAG 2160
GGCAGCCGCC GCACGTAGGC AGCGTCCCCC AGCCCGGGAC CCGCAGGAAT GCGAGGGGCA 2220
AGACAGATCG CCGGAGGAGC AGGGGTCAGA AGTCAGTGTT TAACCACTCA CTGGCTTTCG 2280
GTGAAGCCAG AATGTTAGCA GCGAGTCGCG GTCGGGGGCC TTGGGGTTGC ACACGCTTGC 2340
TCCAAGCACC GAGGCTCAGC TGAGCACATG CACAACCCTC TCGATGCAGC GGAAAGTCGT 2400
GTGGCTTAGG GCCGCACCCC GAATTTCGCC GCACCCGCCG CTGTGCCATT TACAACCCCC 2460
CACCCCGCCA CTGCTGTCAC GTAGCAATCA AGAGTAAAGG TTATCACAAA GTCTGTTCTT 2520
CGAAGGAAAG AGTTGGAATC AAGGACTTCG GACGGGAGGA AGTTGGTAAG TTACCGCTTC 2580
CTCCCTCCTG TTTTCCTCTC CTTGTTTAAC TTCTCACAAG AACATGTGGC AGCGCTGCAG 2640
GTTAACTCAT CTTACATAAC TTCGGGGCCG TGTCAACTGT TCAGAAGAAA GAAAAACAAG 2700
TATTCTCTTC TGTAGAAGTT GTATTTAGAA ACAGGCTCTG TTGTTTAGGA CAAGTTCACT 2760
TGTGTTGCCT GATCACTTGC AGCAGAAAAT CTTAGAACTG CTCCTCAAGC AACAAAAAGT 2820
AGGGGCTCCC ATTTCCATCT TTCTTTCTTT TCTTTTTCTT TCTCTCTCTC TCCTTCCCTC 2880
CCTCCCTCCT TCCTCTCTCT CTCTTTCTTT CTTTCTGATG GAGGCTTGCT CTGTCGCCCA 2940
GCTGCAGTGC AGTAGCACGA TCTCAGCTCA CTGCAACCTC CGCCTCCCGG GTTCAAGCGA 3000
TTCCCCTGCC TTAGCCTCCC GAGTAGCTGG GACTACAGGT GCGCACCACC ACGCCCAGCT 3060
AATTTTTTGT ATGTTAGTAG AGATGGGGTT TCACTATGTT GGCCAGGATG GTCTCGATCT 3120
CCTAACTGCG TGATCCGCCT GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGCC 3180
ACTGTGCCCA GCCGGGCTCC 3200