EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS182-21675 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr9:93953760-93957160 
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
AATTGTTTTA AAAGAGCTGT TTGGAGTTGA GGCGCACCTG CAAAATTAAA CACACCAGGG 60
TGAGAAAGGC TTTCTGGGGG CGGATCTGCA GGACTTGATT TTGCTGAGTT TAATGCCACT 120
CATTTCACTT TCTGTTGGCC AGAGCCCGTT TCCCCTGCTT GAAGGCACAG AACCTTGCTG 180
GGAGCCAGGC AAGCTCTCTG GACGGGATGG GCAGCCCCAG GGCCAGCCAT CCCAAGTCTA 240
GGGCTTGCTG GGGCCTAGAC TTTTGACCTC CAAAGGGTAC GGAGTCTGGG GACCACTCTG 300
CACACCATCC TCCATCCAGA GAGAGGGGCC ATTTCCATCC TCATTCGGTT TCCCATATTC 360
AGGGGAACTC CTCTCCAAGA AGAAACAAGG GCTCAGTTCC ATTTCTGACT TCTCTCTAGG 420
TCAGCACGTG CGGTCACTTC ACAGAAAAAT GGTGTGGATG TGCCAGACTG GGGACAAAGG 480
CCCTCTGTTG TCCCCATTAC CTGTGGTTTC CTGCCACAAA GGCTACACCA AGTACCTTAT 540
AAAGAAGGGC TGAGCGCTTC ATGGATTTAC TCAAAACCCA GCGCTCTGGG CTACTATGAC 600
CCCAGCCACC AACAGGTGTT GAGACTCCCC TGAGGCCCCG CCAAAACTGG CTGGGGTTTC 660
CTCTCCACCT CAGTGCCACC CCTGTCTCCA AGCCCATACT CCCAGGCATC TCTCAATCAC 720
TACCTCTACA AGACCCCAGG GTCTGGGTAA TGGGGGCTGG CAGAGCCTGG ACTCATTCCT 780
GCAATGACGT CGGATACCAG CGGCACCCAT TCCCTCTCCA AAGCTCATGT CCACAAGGGC 840
AAACGATAGC ATCCCCCTCC ACCCCGGCAG TAAGCAGCAG CGAGTCTCAC CAATTTGAGA 900
GTCTCTAGAA CAACAGATGG TAATTTGTTG ACACAAAGAT TTAAGGGGAC TCAATTACAG 960
TCCCACTGAA AAAGCTCTCT CTAAAATAAG AAAGTATACA GATTCCTCAG CTCGCAGAAA 1020
TTGCTGACAG CTTTGTTTTC AACCCTCCAG GAGTAAAAAG AAGCTGACAA CTTATTTTTG 1080
CAGGTTATGC TCATTCAAGT CTATTTTTAG ATCTTGTTCC TAAATAAGTA CACCAGAATA 1140
GCATTCAGTT TGAAAATCAC CATCTGTTCA GAGCAATGAG CTTGGCCTCG CTGGGCTGGG 1200
TATACCTGGC CCATGGCAAG GTGGCAGTCC CCTTGTGGAC TGAACCGAGG GGGCAGTTTC 1260
AGGTCTCCAA GTGGTGTTTG AAGAATGCAC TAAAAACAGT CACAGGCAGT TGGCATTTTA 1320
AATGCCCATT AAACAACTAT TAATATATTT TATTTATAAG CTGAGAACCA CACAAAAAAT 1380
GCCCTTGGCT TTTTAAAAAG AAGTTCAAAT AATCCCTTGT ATTTAAATAG ATTTCTTATA 1440
AAAAGGCGAT CCAGCCTAAG TTTGGTAGTT AAGATAAAAA TTAACCTATG GAAAAGAAAG 1500
CCAGCTCAGA ACGCTATAAA AAGGCCCCTT CCCCCCCCCC CTTTCTTCCG GTGTATGGTG 1560
GCCCTCCCCT CCCTCTGCAG CCACTTGGTA GTGACTCACG CTTTTCTTTG GAAATGCAGT 1620
TGCTGCGTGA AACACAACGT GAGAATGGGA ATCTGACATA TGAGTAACCC GGCCGAGAGG 1680
CACCTCTTGG AAATGACACT GGGCCTTGGC TAGAATTACG CACAGGCCCT GGGAGGGCTG 1740
CGGCTCGTAG GCCCGTAGGG GGCAGGGTGA GGGCGGAGGT CCTGGCGCCC CCAGGCCTGA 1800
CCCGCCCGCA CCGCTGGGCT ATTTTTAGCG TCCACTAAAC TTAGCCGACT CCACCCTCTT 1860
GAATAACCCA CATCTTAAAA TGCTATTTTT CTCCAACAGG TCAAAAGAAT TCTGCGAGTT 1920
AGAGCGCAGA TTAAGTTGCT AGCGACGGGC ATTGAAGGTT TTAGAACCGA GAAAATGAGC 1980
CGGTGGCGGG GAGCGCGTCC TCAGCGGCCA GGCCCGGCAC GGGGCTCGGG CACTCGGGGA 2040
CACACGGTGG TCGTCGCTGT GTCTCAGCAG GACCCTGTGC GCTGGAGAGC TTGGGGCCGC 2100
GAGTCGCGCA GCAAGGAGGC TTCTGGCTTC TCTATTTTTA GCCTCTGAAC GTTTTCCAAA 2160
ATAATTACCA AAAGGAAATA CACACGCACA CATGGACCTA ACACACAAAA CGTCCTTCTG 2220
CGGGAAGCCA GCACTAGGAA AGAAAAAAAA AAAAATCCGA AGTGAAATTA TGACACAGGG 2280
TTTTGTAACC CGCGGTGGCG CGCTTCTGAA ACCCGAGCCC GGCAGCGGCT TCTTATCTGC 2340
ACCGCGTTCC AGGAAGCAGC CGGCGTTTCG GCCGCGCAAG GGCAGCCGCC GCACGTAGGC 2400
AGCGTCCCCC AGCCCGGGAC CCGCAGGAAT GCGAGGGGCA AGACAGATCG CCGGAGGAGC 2460
AGGGGTCAGA AGTCAGTGTT TAACCACTCA CTGGCTTTCG GTGAAGCCAG AATGTTAGCA 2520
GCGAGTCGCG GTCGGGGGCC TTGGGGTTGC ACACGCTTGC TCCAAGCACC GAGGCTCAGC 2580
TGAGCACATG CACAACCCTC TCGATGCAGC GGAAAGTCGT GTGGCTTAGG GCCGCACCCC 2640
GAATTTCGCC GCACCCGCCG CTGTGCCATT TACAACCCCC CACCCCGCCA CTGCTGTCAC 2700
GTAGCAATCA AGAGTAAAGG TTATCACAAA GTCTGTTCTT CGAAGGAAAG AGTTGGAATC 2760
AAGGACTTCG GACGGGAGGA AGTTGGTAAG TTACCGCTTC CTCCCTCCTG TTTTCCTCTC 2820
CTTGTTTAAC TTCTCACAAG AACATGTGGC AGCGCTGCAG GTTAACTCAT CTTACATAAC 2880
TTCGGGGCCG TGTCAACTGT TCAGAAGAAA GAAAAACAAG TATTCTCTTC TGTAGAAGTT 2940
GTATTTAGAA ACAGGCTCTG TTGTTTAGGA CAAGTTCACT TGTGTTGCCT GATCACTTGC 3000
AGCAGAAAAT CTTAGAACTG CTCCTCAAGC AACAAAAAGT AGGGGCTCCC ATTTCCATCT 3060
TTCTTTCTTT TCTTTTTCTT TCTCTCTCTC TCCTTCCCTC CCTCCCTCCT TCCTCTCTCT 3120
CTCTTTCTTT CTTTCTGATG GAGGCTTGCT CTGTCGCCCA GCTGCAGTGC AGTAGCACGA 3180
TCTCAGCTCA CTGCAACCTC CGCCTCCCGG GTTCAAGCGA TTCCCCTGCC TTAGCCTCCC 3240
GAGTAGCTGG GACTACAGGT GCGCACCACC ACGCCCAGCT AATTTTTTGT ATGTTAGTAG 3300
AGATGGGGTT TCACTATGTT GGCCAGGATG GTCTCGATCT CCTAACTGCG TGATCCGCCT 3360
GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGCC 3400