EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-52900 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr7:104643460-104645230 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr7:104643620-104643631ACAGATAAGGA-6.14
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00068chr7:104640205-104646105Adipose_Nuclei
SE_01317chr7:104643698-104644062Adrenal_Gland
SE_02401chr7:104643602-104644601Astrocytes
SE_09206chr7:104640002-104645287CD14
SE_10864chr7:104616513-104659294CD20
SE_13343chr7:104643503-104644664CD34_Primary_RO01536
SE_13343chr7:104644689-104645456CD34_Primary_RO01536
SE_17321chr7:104640196-104645104CD4p_CD25-_CD45RAp_Naive
SE_17808chr7:104642435-104645231CD4p_CD25-_CD45ROp_Memory
SE_18292chr7:104642194-104645719CD4p_CD25-_Il17-_PMAstim_Th
SE_19174chr7:104643312-104644807CD4p_CD25-_Il17p_PMAstim_Th17
SE_19993chr7:104643502-104644660CD56
SE_22301chr7:104643208-104645171CD8_primiary
SE_23122chr7:104643576-104644436Colon_Crypt_1
SE_23859chr7:104643778-104644068Colon_Crypt_2
SE_24813chr7:104643934-104645267Colon_Crypt_3
SE_25859chr7:104641718-104645502Duodenum_Smooth_Muscle
SE_27016chr7:104643567-104644732Esophagus
SE_29643chr7:104644036-104644966Fetal_Muscle
SE_31663chr7:104643492-104644460Gastric
SE_36165chr7:104643180-104644866HMEC
SE_37694chr7:104643018-104645069HSMMtube
SE_40784chr7:104643359-104644825Left_Ventricle
SE_42422chr7:104643498-104644752Lung
SE_44567chr7:104643220-104645308NHDF-Ad
SE_44893chr7:104643446-104644567NHLF
SE_45643chr7:104642256-104645360Osteoblasts
SE_48226chr7:104643379-104644568Psoas_Muscle
SE_48958chr7:104643560-104644488Right_Atrium
SE_50386chr7:104643451-104644524Sigmoid_Colon
SE_51149chr7:104640498-104646174Skeletal_Muscle
SE_52080chr7:104643523-104644361Skeletal_Muscle_Myoblast
SE_52568chr7:104643489-104644523Small_Intestine
SE_56655chr7:104644089-104645186u87
SE_60468chr7:104643384-104663776DHL6
SE_62336chr7:104643373-104663239Tonsil
SE_63872chr7:104643503-104644582HSMM
SE_64355chr7:104642677-104645163NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7104643466104644268
Number: 2             
IDChromosomeStartEnd
GH07I105004chr7104645120104645389
GH07I105002chr7104643041104645002
Enhancer Sequence
GTATAGACAC AGATTGCCAG TGTTACATGG ATTCTCAGCA TAAAACTAAA ACTTCAAGAA 60
CTCTCTAAGT CCGTGTTTAT TAATAGCAAT GACAACCAAT TATCCAATAT CTAATGCTGT 120
CAGGTAGCAA GCTACACATT TGTAGATAAT CAAACAATTT ACAGATAAGG AAACAGTTCA 180
GTGAAGTAAT AAGATCATGC AGCCTGTAGT AGGTGAGTGT ACTGGGAAAG GAAGTCTGAC 240
ACTTAAAACT CATGCTTGCT CCTAATTTCA TTTCATTTCT TTTCTTTGGA GACAGGGTCT 300
TGCCCTGTTG CCCAAGCTGG AGTGCAGTGG CGTGATCACA ACTCACTACA ACCTCTGCCT 360
CCCAGGTTCA AGAGATCCGC TTGCTTCAGC CTCCCAAAGT GCTGGGATTA CAGGAGCATG 420
CCAGCACGCC AAGCTAATTT TTGTATTTTT AGTAGACACG GGGTTTCACG ATGTTGCCCA 480
GGCTGATTCT GAGCTCCTAG ACTCAAGGGA TCCACCCACC TCTGCCTCCT AAAGTGCTAG 540
GATTAGTCAT GAGCCACTGT GCCAGGCCAA TCTCTTTTTA TGTACAACAA GGAAGAAAAA 600
AATGTAAGAA TCAAGTACTT TTTCTAATCT TGATTCCATC CAAGTTAGAT TAGAAATGAG 660
ATCTTATAAC CCAGTATACA ACAGACTCTT TACTGACTGT CCTATTTTCA ACTTAGAGGT 720
AGAACAGCAA TATTTAGGGG TTCAGGCCTG GCTCTGTCCC CCATTACACT GCGACTCAGT 780
CAGTCATTTC CCTGAGACTG TTTCCTTAAA TATAAAAGAA ACAAAATAGA GAAAGTAGTG 840
GCCTAAGACT CACAGAAAAA AAGACTCCAA ATTAAAAATA AAATAAAATT ATGTGGTCCA 900
ATCCGCCCCC TTTCCAGTCT CATCTCTCAA TGTACTAGGT CACACAAGCC CAGTGAAATT 960
GGTTTACTTA AAACATTGTC TCTGTTACTG TTTTATGCCT TTACACATAA AACCATGCTG 1020
ACTGCAAATA TGTTGTACTC TACTGCCCCA CCCTTTCCCT AATGAAACCC AGAACTATCT 1080
GCCTCCTAAT CCAAAAATTC TATTTCCTCT GTGAAACACA TTACCCCATG AACTGGGATA 1140
TCTGGCTGAA TGCTTACAGT ACTTGGTTAC TTACTGATGT GGCTTAATCC CAAACTAGAT 1200
TATAAATGAA TAGAGTAGGG ACTAGTCCTT CTAGCTTGCA ACAAAATAGA TACATGTTTT 1260
TGAAAAGTGT GGGAAAACCC TCTGAAGTCT TACAAGATGA TGGTATAGAA TCAACCAGAC 1320
CATTTGCATC AAATTTTATA TTCAAGGGAC TTTCTATTGT AATAAACACA TACTATGGGC 1380
AACATTTTCA GGCATCTGGC ATCAAAGCAG ATTATCTATT CATTTGTGCA ACAAAACTGC 1440
ATGCCTATTA CATGCCAGGA ACTGTGCACT TCAGCCATAA AGATGAAAAA CATTGTGTCT 1500
ATCAAGATCT CATATACTAA TGGAAAAGAG GAACATGAAC ATGACAGCAT GATAGGAACA 1560
CATGTTAACA AATAGAAGGG AATGTCTTAT TTTCTGGACC AAAAAAAATT GGGATTACAA 1620
ATCAATAATT GCTCCTGAAA GGTTTTATAT CTAATTTAAT TCTTAACGCC ATTATATAGT 1680
TAATATTTTA CCTGCTGTAT GGATTATAAA ACTGAGTCCC AGAAAGCAAA CTACCTAAGT 1740
CTTCCTTGAA GTGGAAGTGG TATTCAAACT 1770