EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-31017 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr9:130280530-130283140 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr9:130282133-130282150TGGTTTCCTAGAAACCA-6.09
CDX2MA0465.1chr9:130280749-130280760AGGCCATAAAA+6.02
STAT1MA0137.3chr9:130282136-130282147TTTCCTAGAAA-6.14
Stat4MA0518.1chr9:130282133-130282147TGGTTTCCTAGAAA-6.21
ZfxMA0146.2chr9:130282954-130282968GAGGCCGAGGCGGC-6.02
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00872chr9:130279917-130281272Adrenal_Gland
SE_00872chr9:130281479-130282530Adrenal_Gland
SE_00872chr9:130282713-130285433Adrenal_Gland
SE_01693chr9:130281478-130282520Aorta
SE_02373chr9:130281347-130285497Astrocytes
SE_06387chr9:130282789-130285496Brain_Hippocampus_Middle
SE_26528chr9:130280176-130281238Esophagus
SE_26528chr9:130281410-130282592Esophagus
SE_30306chr9:130281361-130282642Fetal_Muscle
SE_31422chr9:130280488-130281325Gastric
SE_31422chr9:130281467-130282502Gastric
SE_31422chr9:130282723-130285455Gastric
SE_36116chr9:130280649-130282794HMEC
SE_37370chr9:130279973-130288932HSMMtube
SE_38118chr9:130279758-130285472HUVEC
SE_39322chr9:130282716-130285479IMR90
SE_42140chr9:130279268-130281346Lung
SE_42140chr9:130281461-130282698Lung
SE_44201chr9:130281385-130282642NHDF-Ad
SE_44773chr9:130280048-130281309NHLF
SE_44773chr9:130281328-130282632NHLF
SE_44773chr9:130282674-130285466NHLF
SE_45705chr9:130278751-130289381Osteoblasts
SE_47421chr9:130280368-130282656Panc1
SE_47421chr9:130282794-130288144Panc1
SE_48868chr9:130281419-130282559Right_Atrium
SE_50184chr9:130281471-130282643Sigmoid_Colon
SE_50184chr9:130282690-130285451Sigmoid_Colon
SE_52096chr9:130281838-130282688Skeletal_Muscle_Myoblast
SE_52507chr9:130280660-130281300Small_Intestine
SE_52507chr9:130281404-130282514Small_Intestine
SE_53712chr9:130281376-130285445Spleen
SE_55718chr9:130279625-130285401u87
SE_63712chr9:130280432-130281082HSMM
SE_63712chr9:130281328-130288557HSMM
SE_65259chr9:130279510-130281152Pancreatic_islets
SE_65259chr9:130281365-130282623Pancreatic_islets
SE_65259chr9:130282863-130285459Pancreatic_islets
SE_67788chr9:130279625-130285401u87
SE_68760chr9:130280020-130281181H9
SE_68760chr9:130281424-130282590H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9130281582130281994
chr9130282829130282995
chr9130281041130281204
chr9130281492130282485
Number: 1             
IDChromosomeStartEnd
GH09I127516chr9130279143130288428
Enhancer Sequence
AAGAGACAAC CGTTAGGGGA CAGGCCACGG GCCCAGGGTC ACAGAGCAGG GAGTGGCAGA 60
GCCAGGACTA AAAGCTCCCG TCCCATAAGC AGCCACCCAG AATGGCCCTA GAGGCACCCA 120
GAGACCCTTG TTCGAGCCCC AGTTCCTCCC TTACTGCTAG ATCAGGGCCC TTCAAACTTT 180
GCCTGGAACA GGCTAGGCAG CAGATATTCT CAGCCCGGCA GGCCATAAAA CCCCTCCCGC 240
AATGCTCGCC TCTACAGTCA CAGCACAAAA ACAGCCACGG ACCATCCAGA AACAAATGAG 300
CGTGCCTCTG CTCCAATAAA CTTTGTTGAC AGAAACAGGC AATTGGCTGA TCTGGGCCCA 360
TAGGCCATAG GTTTCAGAGC CTGGTTCTAG ATCACTGAAC CCGAAATGGC CTGTTTCCTC 420
TTCTGAACAA TGGAACAATG GCCTCACAGG TCCACTGCGG GGCTCCCTGG GCCACAGTGT 480
AGGGACAGGA GATCAGGGTC CAGCACTGCT CTGCGCCACA CTTTTTATCA ATAACTGAGG 540
AGCCAGCTGC CTGCCCCACT GGGCCCGGGG TCTGTCCTGT TACTGCTAAG TCCAGGTCAG 600
TACCTGGCAC AGATGCTTGA ATAACTTTGT TAAAGAATGA AGCTGGGTGT GGTGGCTCAT 660
GCCTGCAATC CCAGTACTTT GGGAGGCTGA GGTGGGGGAA ATCACTTGAG GTCAGGAGTT 720
CGAGACCAGT CTGGCTAACA TGGCAAAACC CCATCTCTAC TAAAAATACA AAAATTAGCT 780
GGGCATGGTG GCAGGCACCT GTAATCCCAG CTACTAGGGA GACTGAGGCA GGAGAATCGC 840
TTGAACCCAG GAGGCAGAGG TTGCAGTGAG CCGAGATTGC GCCACTGCAC TCTAGCCTGG 900
GCAACAGAGT AAGACTCTGT CTCAAAAAAA AAAAAAAAAA AAAAAAAAAG AATGGAAGAG 960
TTTGCTATTA ATAACAGCTA GAAGAACACC ATTTCTGAAT TTTTGTCACT GTTGGTGCTG 1020
TCAGTGGCCC AAACGCCAGC AAGGTAAACC CCTGAGTGAG GCGTGGACCT CCAGATTCAG 1080
TGCCCGGGAG GCAATTGGCA GGAAGTTACA AAATCTGACT TGGGGTAAGA AGGTGGTCAA 1140
ACGCCACCGA GCCAGGCAGC AGGCAGACTC CCCTGGCCGC GTGCCTCTGA CCACCGCATC 1200
CCCAAAGCCC AGGAAGGGGA AACGGAAGCC TGTGCATCAG AAACCTAAGG CTCCCACTGC 1260
CATGACTATG GGCTGAGTCA CCACCGGCAG AGAAAAAGCC CCTCTCTGGG TCCCTCCTCT 1320
CCCCACACCC AGCTGACCAC AGAAATCACT GCCTGTCGGA GCCGGGAGGG AGCTGAGCAG 1380
GGGGAGGCCC AGCCCTCATC CCTACAGCGC AGCTGCCTGG ATGGGGACGG GGGCCTGTGG 1440
GAGTCTCACT CCTGCATTTC AGAGACCTGA AGTCAGGCAG GAGTGACAGG AGCAGGGCAG 1500
GGATGTTCCA GCTGGAGCAG CATGCAGAGC CCTGGGTGGG GGCTGCCCAC CTGGGCCAGG 1560
GAAGGAGGTC CCCCCGCCAC CCCACCCGCC TCTCAGAAGG GCATGGTTTC CTAGAAACCA 1620
AGTTTTGACT GGAAAATCTG GACAGTGCGT TACCTGCAGG CACTCCCACG GGGAGAGGGA 1680
ATTTTCATCC TGCATGCACC AAGTCAGGTG TGCAGGGCAG GCCTGCTTTC CAGGTGGCGA 1740
GAAGGTGAGG CAGAGGGCCG GGACAGCGGG AGGGAGGCCA GCCAGCCTTG ACCCTTGGGA 1800
TTCTCTCTTT CTGCACACCC AGCCGCTGAG TGTGACAAGT TTCAGGGTCA CCCCTCCTGA 1860
GCTCTTCCCG TGAGCCTAGC TGTTAGGGGC TGAAGTGTGT CTCCACACCC CCCAAATTCA 1920
TATGCTGGAG TCCTAACCCC CAGTACCCCA GAACGTGATT ATATTTGGAC CCAGGGTCTT 1980
TTTTTTTTTT TTTTTTTTTT TTTTCTGAGA AGAGTCTTAC TCTGTCGCCC AGGCTGGAGT 2040
TCAGTGGTGC AATCTTGGCT CACTGCAGCC TCCGCCTCCC AGGTTCAAGC CATTCTCCCG 2100
CTTCAGCTCC CAAGTAGCTG GGACTATAGG CACCCGCCAC CATGTCCAGC TAATTTTTGT 2160
ATTTTTAGTA GAGATGGGTT TTCACCATGT TGGCCAGGTT GGTCTCAAAC TCTTGACCTC 2220
AAGAGATCCA CCCACCTCAG CCTCCCAAAG CACTGGGATT ACAGGCCTGA GCCACCGCAC 2280
CCGCCCTTGG TCCTAGAGTC TTAAAGAATT AAGTTAAACA GAGGGGATGA GGATGGGACC 2340
AAATCCAATA CAACTAGTGC CCTTAAAAGA ATAGTACATT TTGGCCGGGC ACAGTGACTC 2400
ACGCCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCGGCAG AATCACGAGA TCAGGAGATC 2460
AAGACCATTC TGGCTACAAA AAATTAGCCA GGTGTGGTGG CACACGCCTG TAGTCCCAGC 2520
TACTCGGGAG GCTGAGGCAG GAGAATCACT TGAACCTGGG AGGCGGAGGT TGCAGTGAGC 2580
CGAGATTGCG CCACTGCACT CCAGCCTGGG 2610