EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-21927 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr14:104345480-104350270 
TF binding sites/motifs
Number: 14             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF1AMA0046.2chr14:104346560-104346575GTTTAATCATTAACG-6.11
HNF1BMA0153.2chr14:104346561-104346574TTTAATCATTAAC+6.07
HNF1BMA0153.2chr14:104346561-104346574TTTAATCATTAAC-6.48
LMX1BMA0703.2chr14:104350241-104350252TTAATTAAATT-6.32
Lhx3MA0135.1chr14:104350238-104350251AAATTAATTAAAT+6.07
NR2C2MA0504.1chr14:104345676-104345691TCACCTCTGACCTCC-6.64
Nr5a2MA0505.1chr14:104345957-104345972GGTGACCTTGAGGTC-6.01
PHOX2AMA0713.1chr14:104350242-104350253TAATTAAATTA-6.62
PROP1MA0715.1chr14:104350242-104350253TAATTAAATTA+6.32
PROP1MA0715.1chr14:104350242-104350253TAATTAAATTA-6.62
Phox2bMA0681.1chr14:104350242-104350253TAATTAAATTA-6.62
RARA(var.2)MA0730.1chr14:104345948-104345965AGACCTCTTGGTGACCT-6.16
ZNF263MA0528.1chr14:104347154-104347175GCCTCCTCTCTCTCCTTCCCC-6.1
ZNF263MA0528.1chr14:104347155-104347176CCTCCTCTCTCTCCTTCCCCC-6.31
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_23468chr14:104345587-104348167Colon_Crypt_1
SE_23468chr14:104348973-104349933Colon_Crypt_1
SE_23954chr14:104345647-104348544Colon_Crypt_2
SE_23954chr14:104348857-104349930Colon_Crypt_2
SE_25046chr14:104345583-104348736Colon_Crypt_3
SE_25046chr14:104348779-104350092Colon_Crypt_3
SE_27368chr14:104345831-104348009Esophagus
SE_31562chr14:104345148-104349843Gastric
SE_35645chr14:104344906-104349032HepG2
SE_41155chr14:104345570-104348944Left_Ventricle
SE_41955chr14:104345669-104348619LNCaP
SE_42764chr14:104345567-104349607Lung
SE_47527chr14:104345562-104348703Pancreas
SE_47527chr14:104348918-104349418Pancreas
SE_50688chr14:104345110-104348321Sigmoid_Colon
SE_54304chr14:104345470-104350010Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr14104348846104349086
chr14104349336104349761
Number: 1             
IDChromosomeStartEnd
GH14I103879chr14104345172104349612
Enhancer Sequence
ACTAAAAATG CGAAAATTAG CCAGGCGTGG TGGTGGGGGC CTGTAATCCC AGCTACTCGG 60
GAGGCTGAGA CAGGAGAATT GCTTGAAACC GGGAGGCAGA GCTTGCAGTG AGCTGAGATG 120
GTGACATTGT ACTCCAGCCT GGGCAACAGA GTGAGACTCC GTCTCAAAAA AAAAAAGAAT 180
ATGTTTACTT TCACACTCAC CTCTGACCTC CTCTTGGGAA GACGAGGTTA CCGGTGCCTT 240
CCCTTCTCTT CCACTTTCAG ATTTCTTCCC GGTCAGCCCC AAACACTGAA TGTAAATACG 300
GTCCAACATC AACCTGCAAA CGAACACTGA CATGAAAGTG CAGTTGGAAA GGATCTCGCA 360
AAGGAACAGA ATCTGGTGAT CCTAATCGTA ATGAACGTGA TCGCCGGGTA TTGAGAGCTT 420
GCAGGTACCA GGGCTCCGGC ACTACGTGTT TCACAGGGGC CACTCGGTAG ACCTCTTGGT 480
GACCTTGAGG TCAGGTACCA CGTTCCCATT TTACAGAGGA GGAAACTGAG ATAACCTACG 540
ACAGCGAAAA GGTAGCAGAG CTGGGACTGG TGCCCAGGCT CGCCGAGTGG AAAAGCCCTC 600
GGCCACCGTG GAGAGCTCGC TTCCTGTGGT CTGAAGCGTC GCCCCTGCAC CGGCTTCTGC 660
TGCCAAGGAT GGCTTTTCCT CACTGGTGCC CACCTACGCT CACTTGTGTC ATGTGGTTAA 720
GCCCTTTTGG CAACATAAGA CCTTTCCCAA GAATGTGCCT CGGTGCAGAG GAAGACGGTG 780
GGGGCAGGCC CCCTCCCCGG GATGCTCCAC CCTCCCTGAC CTCACACGGG TGCAACCTGG 840
GCCGTGGCCG AGACCTGCTG TGTGGCAGAC AATGGGAAGC CTGTGTGTCG TCCTGGGTGC 900
CGGATTTAGA CAATATTTAG CTTTCCCTTG GTGGAAAAGC CTTTCCCCTC CTGCTTTGGG 960
CAGGAACTGG TTCCTGTTGG GCGGGGCCTG GCTGCTGCCC CACCCCCACC CGGCCGGGCA 1020
CCTTGACCGG CAGCTCTCCG GGCTGCTCCC TGCCTGTGTC CCTGAGCACT GACTCCAGAG 1080
GTTTAATCAT TAACGGGCAC GTTTGGCCTT CGGTCGTGGG CTGGAATTTG GGACCTGTGC 1140
CCGGGAACAA TGATCTCCGA CACATTATTT TGTGTAAAAT CACTTTTAGC TGCCATTAGC 1200
TAATAAAGCT GGAATAAAGT GAGGTCCATT AACCAGCACT GGCCTCTCGG CCTCTGGGGC 1260
TCCTTGGGAG GGACCCAAGG GACTCACCTT TTGAGGACCG TGAAATCGCC GCTAGAAAAT 1320
GTGCTTACAA TTGTGGTCCA GCACTGAAGC TGCTCAGTAT GTTTTCAGTC CCCTCTGTGG 1380
CAACCCCGTG TGTGGTTTTG GGGACTGGCA GAGTGCCCTG GAAGCGTGCC CACGTGCTGC 1440
AGATCCACCA GAGGAAATGC TCGGGAAACG CTGACGCCTG CTTTGCCCCC TGTTTCAGGG 1500
TCACCGAATG AGAAGCTGTT GGGATGAATG GCTCCCCCAC CCTCCTAGCC CGGGCCAGGG 1560
GTCGCCCAGC AGCAATGCCC ACCTCCCTTC GTCATGGGAG GAGCTAGTGC TCCAGTCAGC 1620
CCTTTTCATC CTGAGCTGTT TGCTGGAAGT CACCAGTGGG TATCCACAGC GCAAGCCTCC 1680
TCTCTCTCCT TCCCCCAACC TCTGAGACAG CTGGCTGGAT GCTCCCTCCA ACCCCATTCC 1740
CCTGCCCTCT CCTGAGGACA GCTCTGTCGG GAGCAGGGCC TCCCAGCAAG AGCCAGCAGC 1800
TGCGCTGTTT CTGCTGCTCC AGCATTTCGG GGGCAGCTGG CTGGAAGGGT AGGGGCGATT 1860
TAGAGAGGCC CACTGGCAGG TGTGGTGATG GGACTCCATG TCTCCCGCAT GGGACGCCCC 1920
CTCCTCCCTG GGCTTCATTC TTAGGGTCCC CAGTCATTCT TCCCTGGGCA CAGCCCTCCC 1980
TCTCTGTGCC TCATTAGCTC ATCCCCAAGT CCACCCTACA GCTGGTCACC TCCGTCTTGG 2040
TGCAGCCTGC CTCCATGGCC CCGCCTGAAT GCTGAGTGCC CAAGGGCCAG TGTTGCAAGG 2100
GGACCCCACC AGCCTTTCTA CAGAGGCAAC CAGAACCCTC TGGCCTCTCC CCATCTTCCT 2160
GCCCTCCCAC ATTTCTGCCT CCCTAGCTCT GCCCCCTGCC CCAGGAAGCT GAGGCTGCAA 2220
ACTCAGAATC TGCCTTCGCC TCTGGTGCGC TGCCAACTCC CCCTTGGGCA GGCCTGTCGC 2280
CTGCAGCCTG TGTCTGTGCT GCCCTCCACT GCCGTGGCAG TGCCCAGGCC AACTGGTCGG 2340
CATGCTTGGG CTCAGGGACA ACTTCACGGT CAGCACGTGG CTGTGCATGG CCTTGGACAC 2400
CTGGAACGTG GAGCCGGTCA GCCAGCAGCT TTCAGACAGG GAGGGGCCGA AGGGTCCAGG 2460
CCACACAGAG GGCCAGGGCC AGCAGCCAGG CACTGGCTGC CACCACCCGT TTTCCCCCAG 2520
CAGCCCTGGG CTCTCCCTTG GTGGCTCTGC TCTGTGACTG CGGGCTGGTT CTTGGACCTC 2580
GGTTCCCTGC TGTTCTGGGA GGCTCGGGGC CTAGCTGAAC TTGGGGCCTT CCTGCCTGCC 2640
AGCCCCTGAC TCCGGATGGC CAGACACACT CCCAGAAACT CCACCCGGCC TCTTGTTGGC 2700
CACCGGAAGG GCTGGCGAGA GCTGCAGGAT GCGCACACCC CTATTGAGGG CTTGCCCGCT 2760
GCCCCTCTGG GAGCCTTCCT GGAATCCGGG AAATGAAGGC GCTCTCAGGC AGGACACCCA 2820
GTCAGATCCG TCTCGTGCAG GGCTCCGGGC CCCGTTCCTG GCCCTGCCAG GGAAGCCAGA 2880
CCCGGCTGCC CAAGAGCAGA CCCTGCCTGC AGAAGCGCTC CCAGGGGAGA CAGCCAGGAC 2940
CTCACTGGGA ACAGACCCCC CAGGTTATTT CCAAGCCTGC CCCTCCTTTG CCTCCCTGCT 3000
GCCTCCTCAT ACCCCCCCCG CACCCCGGCT GAGAGCAGCC ACCGCCCAGC TTGCCCTGCC 3060
ATGGTTCTCT GCTCAGGCTA CAGCCCCCTG GATTAGAGTG GTTTACTGGT CTCTGCTACT 3120
TTTAGGATCA AACCTAAACT CTTAAAGAAC TTGACCCACA AAGAGCTGGC TCTGCAGATC 3180
CGTGGGGGAA AAGGTAGACT ACTCTGTACA TAGGGTTTGG ACAACTCTCA AGAGAGAAAG 3240
CTGGTTTATT TCACATCACT GGGAGAGATC CACTCCAGAG GGATTAAATA ACTTACAATA 3300
TAGAAAATAT TCGAGTGTGG GCCCTCCTTC ACCCCCAAAG TGGGGTGGCT CTCCAGGGTC 3360
ATCACTGAAA ACACTCGATT GCATAAAAGC CCCGTCGGCT CTGGGCACAG CCAGGAAGGT 3420
GCATCTCCCC AGACAAACAA GCTGTATTAT CTCCAGCATG TAGGACAGGG AGGTGATGTT 3480
CTCCAGATGT TAGGAGCTGC CTCCCACTCC CCGGCCCTGC CCAGGCTGAG TGCCTGCTGA 3540
ATGCTTTATG TAAGTGCCAA ATGGCAGCGC TTGCACCCTG GGGCCGGATG GAACAGCAAG 3600
GAGGCCTCGG GCCTGGGTGG GGGCCTTGGG GCCCTGCTAA CACCATGGGA GGACCTGTGA 3660
GGACCAGCCC TGGGGAATTG CACCTGGCCT CAGGCCCTCC CCTCCTGGCC TGGGACAGAA 3720
CTGTACAGCC TACTCCAGTT CAGTGCCAAG TGGAGCCACT CCTGCAGGGC AGTGGGCTGG 3780
GTAGGGATGC CACATGTGAG CCGCAGTCTT GGCAGGGACC TGGTTAACCT TGCCCTGCAC 3840
GCAAGGTAGT CCCTGGACAC CACAAAGACC AACCGGCTCC AGCCCGGTCC CAGGGAGCTT 3900
GTCTCAGAGA CCGGCAGGCA GGGCAGGCCC GCTTCAGAAG CTGCCCTGAC GGGACATTGC 3960
GCTTGTCGAG GCGACACAGA CAGACCTGAT GCAGCCCCTG CCGCTGCTCT GCGACCCAGT 4020
TCCCTGAGCT TGGCTTCTCT CAGCTGTGGA CAGGGATAAG AATCAGGGCA CCTGCCTCAA 4080
GGGTGGCTGT GAGGGTGAGA TGGCGCAGCC CAGGTGCCCG GACATAGTCA GCACTTGGGA 4140
AGGTGCCCTG GGTGTGCCCC AGGTGCATAG TGCACACAGG GTGGGGATGA GGGGCTCCCA 4200
CAGGTCTGGA AGATTTCCTG GGTCTGCACT GGGTGGCCTG GGCTGACACG TGGGCAAGAG 4260
CACCCTGGCC TGCAGGGCAC AGGATGTACA GAAACTCCAA GGCCAGGGGG ATGGTGAGAG 4320
GCTGTCCCAC TACAGGGCCT GGAGAGCCGC TGTGGTCTGG GAGGGACAGC GTGCCAGACT 4380
TTCCTCCTGG GAGTCTCCTG GCCTCCTGCT GTCTGTCATG ACCGGGAGCC TCCCGGCCTC 4440
CTGCTGTCTG TCATGACCGG GAGCCTCCCG GCCTCCTGCT GTCTGTCATG ACCGGGAGCC 4500
TCCCGGCCTC CTGCTGTCTG TCATGACCGG GAGCCTCCCG GCCTCCTGCT GTCTGTCATG 4560
ACTGGGAGCC TCCCGGCCTC CTGCTGTCTG TCATGACCTC CTCTGGCTCC CAGAAGGCCT 4620
GGGCTAGTTC ATTTCCCCTC AAGATTCCCA AGCCAAGGGT GATGGTGTAT GCCTGTAGTC 4680
CCAGCTACTC TGGGGCTGAG TCAGGAGGAT CACCTGAGCC CAGGAGTTTG AGTCCTGAGG 4740
AACATCTCTG AAAAAAAAAA ATTAATTAAA TTAGAAAACG ATTCTCCCAG 4790